Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Position: Territory Manager, Endo Location : Bangalore, India The BSC Endosurgery Territory Manager will be responsible for driving sales revenue to exceed division priorities, defining and developing new business opportunities that clearly reflect the company s vision and priorities, and functioning in and contributing to overall team success. Individuals will exhibit strong clinical excellence, stay current on products, programs, and competitive knowledge, and be able to face up to program situations quickly, directly, and without hesitation. The candidate will have experience and be comfortable in the hospital and office-based settings and be creative in their problem-solving. The Territory Manager will develop key relationships through frequent and routine customer visits, product demonstrations, product in-services, and procedural observation. Relationships must be established with Physicians, Nurses, Technicians, Hospital Infection control, and Materials Management. Additionally, the candidate will build and maintain constructive strategic relationships in key accounts and be able to take actions that are consistent with the stated organizational goals. The candidate will manage their territory with integrity and in accordance with our Code of Conduct. Responsibilities and Requirement : Graduate with 3+ Years of experience in medical devices. Should have strong communicate skills Develops quarterly plans designed to achieve revenue targets. Clinical excellence in respective disease states. Build sustainable business relationships. Drive sales revenue to exceed division priorities. Define and develop new business opportunities that clearly reflect the companys vision and priorities. Build and maintain sustainable strategic relationships in key accounts. Stay current on BSC products / programs / competitive knowledge. Focused individual committed to building trusting relationships with key physicians and nurses by training, educating and selling them on our cutting-edge technologies. Must uphold all of the quality policies outlined within sales structure consistently and completely. Requisition ID: 602218 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. About the Role: Drive the capital equipment modalities of the Intervention Cardiology business, namely Rotablator and IVUS Imaging. Driving therapy advancement by promotion the usage of these modalities for driving better patient outcomes. Location: Bangalore, India Responsibilities & Requirements: Drive ROVUS therapy advancement across assigned territory in most compliant and efficient way. This will include effective Capital equipment demonstration during live case support, In-vitro Wet heart simulation, presentation on product in-service and execution of ROVUS training for Account Manager s, Cath Lab technicians and HCP s. Effectively implement TAG therapy advancement strategy for the incremental ROVUS consumables business in all BSC ROVUS installations in assigned region. Develop in-depth knowledge on ROVUS Therapy and should have optimal understanding of key competition for IVUS, FFR/DFR and Rotablation therapy. Ability to effectively manage product approvals and availability at new Cath Labs in coordination with BSCI Warehouse and authorized Channel Partners. Work in sync with the IC Sales Team. Achieve assigned overall TAG Target for the territory / region assigned, including Capital equipment and ROVUS Consumables business adhering BSCI compliance policy. Work closely with the IC sales team to identify opportunity in potential accounts as defined in strategic map for Rota, IVUS and FFR. Proactively prepare and work on closure of the CE Funnel leads in coordination with internal and external stake holders. Extend help and support to the Govt (GAM) / Private (KAM) tender management team to ensure that we get qualified in tenders with our technical specifications and win in most compliant way. Periodic review on the CE Funnel Leads in assigned region and timely status updating of the new Capex leads on SFDC portal in alliance with IC Sales Team, Channel Partners and Cath Lab companies. Work with IC Team and ROVUS Academy training team to drive the ROVUS trainings at BSC IAS Facility, COE s and ROVUS Workshops in assigned territory. Communicate and support Service team in getting AMC/CMC quote submitted with the existing installation user facility. Work with service engineer/s to execute the New Capital Equipment installation at user facility and minimize down time of Capital equipment in assigned territory. HCP and Key stakeholders call logging in the SFDC portal on a daily basis Requisition ID: 600835 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. About the Role Work in line with corporate, regional and/or country sales strategies to plan, schedule and execute sales tactics in securing BSC product positioning, market penetration, training, and forecasting against market and sales plans. Reference marketing intelligence and research to properly strategize with sales team to capture and broaden BSC s market share. Aid the achievement of customer satisfaction and business growth through focused business planning and people management. Location: Mumbai, India Your Responsibilities will include: Industry Knowledge Responsible for providing continuous tools and education to group members to ensure up to date industry, competitor, and product knowledge. Maintains knowledge of the industry and the competition continually seeking information from physicians, suppliers, and others to challenge, modify and prioritize regional strategies. Collects data from their region on competitor s sales tactics and prepares their team to counter them and keeps the marketing organization aware. Maintains awareness of industry trends and their impact on local/regional sales activities. Business Management Monitors region sales performance on an ongoing basis, initiating corrective actions, preparing reports, summaries, analysis and documentation on all aspects of region management. Assists sales support/marketing staff members in activities such as sales promotion, training or market research in planning and executing special projects Ensures the effective implementation of representative customer records, key contacts, reports and company policies Develops and executes sales strategies and activities in conjunction with the Country Sales Manager Plans and controls expenses to ensure sales objectives are met within budget Integrates individual territory plans and account profiles into a broader regional sales plan and coaches sales team accordingly, in consultation with the Country Sales Manager. Prepares quarterly regional sales forecasts and participates in the determination of market potential and sales expense estimates Sales Execution Regularly travels out with each team member, at least 3 days per week, to ensure divisional strategies are fully implemented Ensures effective territory management and account targeting is practiced in each territory Conducts quarterly sales reviews with team and manager, adjusts strategies in accordance with Country requirements. Responsible for developing, implementing and monitoring a region targeting program Shares personal selling experiences in a way that motivates others and teaches applicable skills. Strong selling skills in front of the customer with others present and without taking over the sales process Coaches others in the field on a disciplined selling model. Identifies sales forecast gaps, submits corrective strategies and implements aggressive sales growth Develops and recommends expansion analysis of new field territories Identifies & recommends promotion programs and materials to help support the sales plan & strategy Actively supports corporate/divisional selling initiatives by proactively assisting in the training and influencing their team. C linical Excellence Maintains the skills and knowledge to sell the entire product line to all applicable buying influences and can differentiates each product line against the competitor s products in front of the customer. Creative Economic and Value-Added Solutions Identifies and develops working relationships with the economic buyer in their country/ regions key accounts Facilitation of contract negotiations involving all products within the region Creates a compete bundle of product and value-add services. Evaluates situations as they affect both the account/customer, as well as the country s overall business needs. Helps define negotiation parameters for tough economically constrained customer situations. Building and Maintaining Relationships Maintains contact with major accounts and key relationships seeking to leverage profitable business ventures Assist key customers in the creation, maintenance, expansion and startup of divisionally related educational courses and forums Attend and participate in customer, company and industry sponsored forums and courses Develop and maintain relationships with key BSC functional areas Spends maximum time in the field with each sales representative to support their professional development needs and to maintain and develop strong relationships and understanding of the customer. Quality Spends maximum time in the field with each sales representative to support their professional development needs and to maintain and develop strong relationships and understanding of the customer. As interface to Clients and Customer Service has direct responsibility to facilitate, share documents and process to identify, notify and ensure any complaint or problem are addressed, thereby demonstrating high commitment to Quality in all interactions and behaviors. Drive as needed to support and facilitate any field corrective action related his/her scope. Participates in driving quality awareness in every employee, while guiding the local organization towards improved performance and customer oriented initiatives. Co-ensures that employees are notified of all mandatory training and quality obligations with HR Manager. Tracks completion of mandatory training. Ensures that all products and advertisement have been through the appropriate approval processes, prior to sharing or publishing. What were looking for in you: 8+ years commission sales-based experience with strong feature and benefit, objection handling, key account management skills, team handling. Sales management and/or medical device background preferred. Market development skills: develop programs for sales rep. and customers to develop new technology sales and acceptance. Strategic thinking Requisition ID: 602793 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Maharashtra, Pune Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Purpose Statement Responsible for providing mechanical engineering support in the maintenance of project DHF deliverables in Requirements Management (RM) tool for new and sustaining medical device products (invasive and non-invasive). Key Responsibilities Read and interpret technical drawings, procedures, and protocols. Import and maintains the project documentation in online RM tool throughout all phases of NPD and Sustaining. Investigates and evaluates the compliance requirements driven from organization s QMS/Work Instructions and validate the same in templates developed in RM tool. Investigates and evaluates existing RM tools/technologies - JAMA, Polarion etc. Investigates compliance gaps in project documents and resolve them with project stake holders. Collaborate with cross-functional process, method, and teams to understand and implement solutions to resolve compliance gap issues in documents. Performs validation of patches and versions of RM tool as and when available. Support multiple projects across different time zones - Asia, Ireland, and North America Quality System Requirements In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. For those individuals that supervise others, the following statements are applicable: Assures that appropriate resources (personnel, tools, etc. ) are maintained in order to assure Quality System compliance and adherence to the BSC Quality Policy. Establishes and promotes a work environment that supports the Quality Policy and Quality System. Qualifications Mechanical Engineering ( B. E. /B. Tech) with 8-10 years of Exp Preferred experience in management of DHF documentation during full life cycle of medical device as per ISO 13485, and ISO 14971 Preferred experience in RM tools like JAMA, Polarion, DOORS, Cockpit Knowledge of MS Office Tools - Word, Excel, PowerPoint. Strong attention to detail with good communication skills. Strong strategic / analytical thinking and problem-solving abilities, with a data-driven approach to decision-making. Ability to collaborate and work as a team player. Nice to have experience in product lifecycle management software and tools. Willingness to work in an agile environment. Job Scope and Leveling Guidelines Functional Knowledge Requires solid knowledge of conceptual and technical and/or functional knowledge and procedures within own job function and a basic understanding of these elements in related job functions. Business Expertise Applies understanding of business drivers and how own team integrates with others to accomplish own work. Leadership No supervisory responsibility; may provide informal guidance to new team members Problem Solving Solves problems considering common practice or procedures; determines appropriate action by analyzing possible solutions and their impact on the business or technology using practical experience, judgment and precedents. Works under general direction from more senior level roles/manager Impact Impacts quality of own work and the work of others on the team; works within guidelines and policies. Interactions (and Communications) Explains factual, sometimes complex and potentially dynamic information to others in straightforward situations. Organizes and presents data/ information to influence decision making, primarily to internal audiences. Requisition ID: 602796 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Maharashtra, Pune Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Purpose Statement Responsible for providing product attribute management services for the wide range of data systems at BSC. As part of a group functionally organized under Research and Development, you will manage the material data and product information maintained in global systems used for all products and components. The scope of support includes both existing and new products from multiple divisions. The work is task-based and will provide support to multiple projects at the same time and will require interaction with cross-functional team members from R&D, Packaging, Labeling, Supplier Engineering, and Operations. Members of the team execute workstream activities based on priorities and to meet business deadlines. Key Responsibilities Reach out to suppliers to help them understand the BSC process and requirements Review, interpret and enter information provided by suppliers for engineering accuracy and adherence to global material standard designations Utilize corporate software tools to query the global material database to search for information Collect data from internal sources and enter into the database Verify information in the database is accurate Work with little to no supervisory work direction to enter, obtain or create complete and accurate material composition information on assigned components Consistently create and maintain highly accurate product data at all times. The material information created is used globally, so high-quality work is of utmost importance. Communicate effectively verbally and in writing with internal team members about the status of assigned component assessments Help develop reports and analyses Support initiatives for data integrity and normalization Generating reports from single or multiple systems for analysis Quality System Requirements In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. For those individuals that supervise others, the following statements are applicable: Assures that appropriate resources (personnel, tools, etc. ) are maintained in order to assure Quality System compliance and adherence to the BSC Quality Policy. Establishes and promotes a work environment that supports the Quality Policy and Quality System. Qualifications Mechanical Engineering ( B. E. /B. Tech) with 8-10 years of Exp Preferred experience in databases and data management Educational or work experience with environmental, health, waste and material regulations or standards pertinent to chemical composition of materials Knowledge of medical device industry or products Previous experience in a regulated industry Ability to analyze data and draw meaningful conclusions from them Excellent interpersonal skills Ability to work with stakeholders to assess potential risks Familiarity with Back-Office roles within multinational companies Relevant experience as user of Quality Systems and ERPs Ability to collaborate and work as a team player. Nice to have experience in product lifecycle management software and tools. Willingness to work in an agile environment. Job Scope and Leveling Guidelines Functional Knowledge Requires solid knowledge of conceptual and technical and/or functional knowledge and procedures within own job function and a basic understanding of these elements in related job functions. Business Expertise Applies understanding of business drivers and how own team integrates with others to accomplish own work. Leadership No supervisory responsibility; may provide informal guidance to new team members Problem Solving Solves problems considering common practice or procedures; determines appropriate action by analyzing possible solutions and their impact on the business or technology using practical experience, judgment and precedents. Works under general direction from more senior level roles/manager Impact Impacts quality of own work and the work of others on the team; works within guidelines and policies. Interactions (and Communications) Explains factual, sometimes complex and potentially dynamic information to others in straightforward situations. Organizes and presents data/ information to influence decision making, primarily to internal audiences. Requisition ID: 602552 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. About the role: The MDM Developer is a critical role in the design and implementation of Master Data Management (MDM) Solutions at BSCI. He/she is responsible for following development standards and best practices, and will assist with requirements gathering/analysis, development, testing, documentation, and deployment tasks with some business-facing. This role will work independently and collaboratively with internal, external, offshore, onshore and nearshore teams. Your responsibilities will include: Develop and support MDM solutions Contribute to a team responsible for designing, developing, optimizing, and maintaining the master data (MDM) processes Understand overall data strategies and roadmaps Assemble large, complex sets of data to meet non-functional and functional requirements Partners with Solution Architects to perform source system analysis, identification of key data issues, data profiling and development of physical schemas for mastering data Follow best practices for data movement, data quality, and master data management Drives the technical design, development, optimization, error handling and support of data management initiatives Create and implement Master Data Management Solutions to ensure data standardization, quality, governance, enrichment and provide a single source-of-truth for the domains Participates in business meetings to understand data through stakeholder interviews and by defining, analyzing, and validating data Perform feasibility analysis, scoping exercises, and works with the project manager to prioritize deliverables Provides mentoring and support for junior developers Collaboratively drafts detailed documentation per standards Working knowledge with informatica in cloud and cloud native MDM Required qualifications: Bachelors Degree in Information Systems, Computer Science, or related field 3 plus years of experience as an Informatica MDM Developer Experience in PL/SQL ((advance queries, tuning) with RDBMS platforms in Agile Experience in Data Integration, MDM, Data Analysis, Modeling and Quality Assurance Proficiency in complex SQL statements and interpret results for accuracy and performance 3 plus years of experience with Informatica ETL workloads Technical understanding of data models, data management, business processes and tools, specifically Data Governance, Master Data Management, Data Modeling, Metadata Management, and Data Quality Working knowledge in MDM life cycle with strong focus on data and with implementing multiple master data domains (Customer, Products, Supplier) using Informatica MDM in cloud and IICS Requisition ID: 588986 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Location: Gurgaon Key responsibilities: Daily Operation Management: AR accounting Credit management Credit limit review Credit limit block AR related month end activities exposure - Bad debt calculation support to ATR team, AR reconciliation, Cash Flow forecasting (preferred) Maintenance of accounting documents filing according to statutory requirements Review credit limits, past due items, AR Dashboard Get Paid tool management Controls Management Perform the corrective and preventive control actions in RCA of incidents Project Management & Value Improvement Ensure controls, DTP, service delivery model, SLA set up correctly before service go -live. Work with team to streamline workflow, enhance operation efficiency and effectiveness through continuous innovation and business process excellence activities within the scope of services deliveredthat result in cost savings and increased service value Work closely with CTC Lead and Project Manager for transition project as required Your Experience MBA/B. com to be considered, non-technical education can be considered with relevant experience. 5-8 Years of experience to be considered. Knowledge on Credit Management Process with CTC E2E process knowledge preferred. Familiar with Credit Reviews systems, agencies & analytical skills Ability to get Credit reports from validated channels and prepare the recommendation based on the authentic data End to end linkages of previous years score depending on the market conditions, goodwill, etc of the customers Fluent English Advanced Excel, Macros, SQL, and other automation technical skill is preferred Very organized and thorough in execution Smart team player and willing to take additional responsibilities Flexibility in working hours Requisition ID: 602459 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. About the Role Sells and promotes company products within a defined geographic territory by developing new accounts and expanding usage of company products by current accounts in an effort to meet a sales quota based on company sales goals and to directly increase sales revenue of the company. Location: Raipur, India Responsibilities & Requirements Sells products by scheduling sales calls to meet with current and potential customers to fulfill revenue and unit growth objectives assigned by company on a monthly/quarterly/annual basis. Develops and implements sales strategies by determining the relevant factors (e. g. , product, competition and pricing needs) of existing and potential accounts to effectively promote the companys products to appropriate hospital personnel and physicians. Develops action plans (i. e. , weekly, quarterly, monthly) by analyzing quarterly and monthly sales figures and reports identifying the needs of particular accounts and discussing issues with Regional Sales Manager to help the organization achieve its annual sales goals. Determines the needs (e. g. , product and pricing), goals, product usage, and types of cases handled by specific customers by meeting with and asking in-depth questions of physicians and other hospital personnel to learn which Guidant products can best address their specific needs. Observes actual procedures in the cardiac catheterization or electro-physiology lab and operating room of hospital accounts to gain insight into the specific nuances of each physician and each member of the lab staff. Establishes pricing packages by working with relevant Guidant personnel to establish price points that address specific customers needs while satisfying company guidelines and policies. Responds to customer needs and complaints regarding products and service by developing creative and feasible solutions or working with other related personnel (e. g. clinical research, pricing and/or marketing) to develop optimal solutions. Develops relationships with hospital personnel (e. g. through casual conversation, meetings, participation in conferences) to make new contacts in other departments within hospital and to identify key purchasing decision makers in order to facilitate future sales. Educates customers on the merits and proper clinical usage of company products by giving presentations and demonstrations using a wide variety of formats and platforms (e. g. , slides, transparencies, manuals) to secure purchasing commitments, often with the help of incentive programs and services made available to the account being developed. Graduate, MBA Marketing (Preferred) 5+ years of relevant experience. Requisition ID: 600986 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Hiring Manager: Prakash M V Recruiter: Palash Sharma Position: Territory Manager, Endo Location : Kochi, India The BSC Endosurgery Territory Manager will be responsible for driving sales revenue to exceed division priorities, defining and developing new business opportunities that clearly reflect the company s vision and priorities, and functioning in and contributing to overall team success. Individuals will exhibit strong clinical excellence, stay current on products, programs, and competitive knowledge, and be able to face up to program situations quickly, directly, and without hesitation. The candidate will have experience and be comfortable in the hospital and office-based settings and be creative in their problem-solving. The Territory Manager will develop key relationships through frequent and routine customer visits, product demonstrations, product in-services, and procedural observation. Relationships must be established with Physicians, Nurses, Technicians, Hospital Infection control, and Materials Management. Additionally, the candidate will build and maintain constructive strategic relationships in key accounts and be able to take actions that are consistent with the stated organizational goals. The candidate will manage their territory with integrity and in accordance with our Code of Conduct. Responsibilities and Requirement : Graduate with 3+ Years of experience in medical devices. Should have strong communicate skills Develops quarterly plans designed to achieve revenue targets. Clinical excellence in respective disease states. Build sustainable business relationships. Drive sales revenue to exceed division priorities. Define and develop new business opportunities that clearly reflect the companys vision and priorities. Build and maintain sustainable strategic relationships in key accounts. Stay current on BSC products / programs / competitive knowledge. Focused individual committed to building trusting relationships with key physicians and nurses by training, educating and selling them on our cutting-edge technologies. Must uphold all of the quality policies outlined within sales structure consistently and completely. Requisition ID: 602219 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Key responsibilities Daily Operation Management: Lead team perform below tasks: Credit management Credit risk assessment Credit limit review Credit limit block Knowledge of Master Data, Collections is preferred AR related month end activities exposure - Bad debt calculation support to ATR team, AR reconciliation, Cash Flow forecasting (preferred) Knowledge of SLA & KPIs preferred Maintenance of accounting documents filing according to statutory requirements Review credit limits, past due items, AR Dashboard Controls Management Ensures all Credit Management activities comply with relevant Acts, legal demands, ethical standards and the internal Quality Management System Review and approve the corrective and preventive control actions in RCA of incidents Project Management & Value Improvement Ensure controls, DTP, service delivery model, SLA set up correctly before service go -live. Work with RPP/GPS and VI Champions to streamline workflow, enhance operation efficiency and effectiveness through continuous innovation and business process excellence activities within the scope of services delivered that result in cost savings and increased service value Act as change management resource to support business for change management communication. Work closely with CTC Lead and Project Manager for transition project as required Relationship Management (Support RM/CTC Lead) Manage day to day interaction with CTC Lead & Local Finance team. Organize periodical meetings with stakeholders to go through service performance and issue resolution Governance meetings & decks data to be shared with CTC Lead Others Be part of Global High Performance Team initiatives as needed Requirements:- University Degree in accountancy or equivalent >10 years experience in business with specialization in finance and operations within a multinational environment Strong knowledge on Credit Management Process with CTC E2E process knowledge preferred. Familiar with Credit Reviews systems, agencies & analytical skills Ability to get Credit reports from validated channels and prepare the recommendation based on the authentic data End to end linkages of previous years score depending on the market conditions, goodwill, etc of the customers Fluent English Advanced influence and conflict handling skills Very organized and thorough in execution Smart team player and willing to take additional responsibilities Flexibility in working hours Requisition ID: 602460 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Maharashtra, Pune; India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. PURPOSE STATEMENT Design, develop and test software applications for medical software products or other software related products for implantable medical device products for RD Division at Boston Scientific. Independently conducts the work as part of a major research and/or development project. Can provide technical direction/review on broad scope or complex projects. Viewed as an expert in one or more in-house technologies. KEY RESPONSIBILITIES Responsible for developing software and/or testing implantable neural stimulation systems or other software related products. Provide competitive advantage in performance, cost and quality. Work on C# applications using technology such as WPF, UWP, SOA (Service Oriented Architecture), and Entity framework Follow the full design life cycle process including driving efforts in requirements specification, design activities, planning, code reviews and creating corresponding artifacts. Provide complete expert engineering solutions to impactful and high-visibility initiatives and projects. Lead and mentor a team of talented Software Engineers. Promote a collaborative environment and pragmatic engineering decision-making. Build collaborative relationships with key leaders and peers, internally and externally, across the organization. KEY SKILLS Strong oral and written communication skills Demonstrated experience in software development lifecycle (Agile), object-oriented design methodology Experience with medical device regulatory guidance such as 21 CFR Part 820, IEC 62304 and ISO 13485 Preferred experience with software configuration tools for source code control (Git), issue tracking (Jira), requirements management (Cockpit), code review tools (Code Collaborator) and 3rd party project build tools ( Demonstrated technical leadership skills Creative / innovative thinker Good organizational and multi-tasking skills Bachelors degree in computer science, electrical engineering, or a related field 10+ years of software development with fluency coding in multiple programming languages, such as C# / .NET Preferred familiarity with Brainlab Surgical Planning Software QUALITY SYSTEM REQUIREMENTS In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. For those individuals that supervise others, the following statements are applicable: Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the BSC Quality Policy. Establishes and promotes a work environment that supports the Quality Policy and Quality System. JOB SCOPE AND LEVELING GUIDELINES Functional Knowledge Requires specialized and comprehensive technical and/or functional knowledge in own job function or field and has full understanding of other related job functions Leverages this knowledge to recommend new and/or improved work processes, typically at an area level impacting various teams Business Expertise Applies knowledge of business and industry best practices and how own area integrates with others to achieve objectives to drive results Is aware of the competition and the factors that differentiate them in the market Leadership Acts as a resource and mentor for colleagues with less experience May lead projects with manageable risks and resource requirements, often broader, cross-functional projects Problem Solving Solves complex and diverse problems, takes a new perspective on existing solutions and exercises judgment based on the analysis of multiple sources of information using specialized knowledge of various alternatives and their impact on the business Works independently within broad guidelines and policies, receives minimal guidance Impact Impacts the ongoing achievement of customer, operational, project/program or key business/organizational/service objectives and recommends improvements within area of responsibility Interactions (and Communications) Explains difficult or sensitive information to facilitate productive discussion; works to build consensus Regularly leads discussions and makes presentations in cross-functional meetings, effectively presenting information to explain recommendations and implications Requisition ID: 600443 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Maharashtra, Pune Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Manager for multiple product development and technology development projects. Provide technical leadership, management responsibility for product design and identification of new technology opportunities. Devotes a significant portion of their time to managerial, leadership, organization and staff development responsibilities: Key Responsibilities: Drives functional excellence initiatives, delivers high quality RD functional. Deliverables, and ensures technical excellence for product or technology development. Drives technical projects of major magnitude and scope. Provides significant guidance and approval regarding technical strategies and approaches. Ensures continued intellectual property development from self and staff. Owns intellectual property development for the product line and technologies. Provides guidance and training to staff, assists subordinates in attaining career goals, motivates individuals to achieve results, and recruits and maintains a high-quality staff. Develops and monitors department budgets Determines appropriate staff levels, schedules and resources. Co-ordinates sessions with project managers/core team leaders to look for opportunities for staff to learn about new initiatives or volunteer on new projects. Drives the development of department tools and methodologies. Determines project staff assignments and schedules work to meet completion dates and RD deliverables. Establishes cross-functional team relationships. Provides an overview of the function and role of his/her group, technical skill sets. Requirement: B.E./ B. Tech or Master in Engineering or Science Minimum 15 + years of experience in System Verification 5+ years of experience with Test automation Medical device development verification experience is preferred Experiences working with ISO 13485, IEC 62304 or any other regulatory environment is preferred Requisition ID: 596590 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Maharashtra, Pune Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Will work independently or as a member of team; design, develop tools and test software applications for software related products. Responsible to ensuring quality of the deliverable and controlling change requests. Key Responsibilities: Designs, develops, debugs, modifies, unit tests, integration tests, automates these tests by using current programming languages, methodologies and technologies. Documents software development and/or test development by writing documents, reports, memos, change requests. Methods used are determined by approved procedures and standards. Tracks software development effort by creating and maintaining records in the approved tracking management tool. Solves engineering problems by analyzing the situation and recommending corrective or alternative actions. Analyzes, evaluates, verifies requirements, software and systems by using software engineering practices. Investigates, researches, selects software designs, operating systems and/or practices. Continuously improves process and work methodologies by interfacing with peers/cross-functional groups and analyzing activities to improve workflow and work processes. Directs support personnel and project activities. Lead Engineers in software engineering activities/methodologies and domain knowledge. Develops and enhances cross-functional team relationships and works cross-functionally to identify and resolve technical and organizational issues. Academic Qualification and Experience: Bachelor s degree in engineering or equivalent (BE, B Tech, MCA, MSc) 12 years of project test development experience with at least 3 or more in test automation development for web-based applications and simulators/emulators. Prior experience in medical domain adds more value Hands-on experience with at least two of the following frameworks Geb/Spock Junit Selenium Java, Groovy Independent contributor who requires less or little supervision Familiar with Agile development methodologies. Preferred Qualifications: Experience automation test developer with Geb/Spock. Experience with change management and issue tracking tools such as JIRA, GitLab. Understanding of requirements, architecture, design, design patterns, OOPs Soft Skills: Excellent Communication, presentation and interpersonal skills with proficiency in English (verbal and written) A positive attitude, innovative and creative thinker Responsible risk taking and risk management xperience of working in a cross-cultural environment Requisition ID: 599435 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Maharashtra, Pune; India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Purpose Statement Boston Scientific is seeking an experienced Principal Cybersecurity Engineer with a strong background in the design, development, and testing of cybersecurity features and controls in a regulated industry. This individual will be responsible for overseeing and guiding the cybersecurity strategy throughout the product lifecycle, ensuring compliance with relevant standards and regulations within the RD Division. KEY RESPONSIBILITIES Responsible for leading the design, implementation, and maintenance of comprehensive security measures across all stages of medical device development, ensuring compliance with relevant regulations and standards while protecting patient data and device integrity Lead the design and implementation of secure architectures for new medical devices, considering connectivity, data protection, access controls, and secure communication protocols Conduct thorough vulnerability assessments and penetration testing on medical devices to identify potential security flaws and implement corrective actions Ensure compliance with relevant medical device cybersecurity regulations and standards, including documentation and reporting requirements. Mentor and guide junior cybersecurity engineers on best practices, security techniques, and emerging threats within the medical device domain Collaborate with cross-functional teams including product development, quality assurance, regulatory affairs, and clinical teams to address cybersecurity concerns KEY SKILLS AND QUALIFICATIONS Deep understanding of cybersecurity principles and concepts, including cryptography, network security, authentication, authorization, and data protection. Expertise in medical device cybersecurity standards and regulations (FDA, IEC 62304, ISO 14971, IEC 81001-5-1) Proven experience in threat modeling, risk assessment, and vulnerability management within the medical device context Strong knowledge of secure coding practices and software development methodologies Experience with penetration testing tools and techniques for medical devices Excellent communication and collaboration skills to work effectively with cross-functional teams Bachelors degree in computer science, electrical engineering, or a related field 10+ years of experience with cybersecurity and software systems Advanced cybersecurity certifications (e.g., CISSP, CISA, OSCP) are highly desirable QUALITY SYSTEM REQUIREMENTS In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. JOB SCOPE AND LEVELLING GUIDELINES Functional Knowledge Requires specialized and comprehensive technical and/or functional knowledge in own job function or field and has full understanding of other related job functions Leverages this knowledge to recommend new and/or improved work processes, typically at an area level impacting various teams Business Expertise Applies knowledge of business and industry best practices and how own area integrates with others to achieve objectives to drive results Is aware of the competition and the factors that differentiate them in the market Leadership Acts as a resource and mentor for colleagues with less experience May lead projects with manageable risks and resource requirements, often broader, cross-functional projects Problem Solving Solves complex and diverse problems, takes a new perspective on existing solutions and exercises judgment based on the analysis of multiple sources of information using specialized knowledge of various alternatives and their impact on the business Works independently within broad guidelines and policies, receives minimal guidance Impact Impacts the ongoing achievement of customer, operational, project/program or key business/organizational/service objectives and recommends improvements within area of responsibility Interactions (and Communications) Explains difficult or sensitive information to facilitate productive discussion; works to build consensus Regularly leads discussions and makes presentations in cross-functional meetings, effectively presenting information to explain recommendations and implications Requisition ID: 600442 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Maharashtra, Pune Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Purpose As a Principal Solutions Rapid Response Consultant GSC Planning COE, you will play a critical role in guiding our Center of Excellence team and the different teams of Global Supply Chain Planning through the implementation and optimization of Kinaxis Rapid Response solutions. You will leverage your expertise in supply chain management and Kinaxis technology to deliver high-quality consulting services that drive tangible business results in the form of quickly designing and implementing technology solutions to address immediate and urgent business needs. Their primary goal is to ensure Boston s Scientific Rapid Response technology infrastructure what can adapt to sudden changes, emergencies, or critical demands. Key Responsibilities Work closely with business users to understand their requirements, challenges, and objectives. Develop strong relationships to become a trusted advisor. Design and architect Kinaxis Rapid Response solutions tailored to meet the specific needs of Boston s Scientific. Ensure solutions are scalable, sustainable, and aligned with best practices. Lead and manage the implementation of Rapid Response solutions, including configuration, customization, integration, and testing. Oversee project timelines, resources, and budgets with the Senior GSC Planning COE Technical Manager II to ensure successful delivery. Provide comprehensive training to users on Rapid Response functionality and best practices. Offer ongoing support and troubleshooting to ensure optimal use of the platform. Stay up-to-date with the latest Kinaxis Rapid Response features and industry trends. Identify opportunities for cusers to enhance their supply chain processes and achieve greater efficiencies. Collaborate with internal teams, including GSC Planning COE workstream leaders and business analysts, product development, and business users, to ensure seamless project execution Follow up and use, implement, and maintain the guidelines of documentation as stated by the Senior GSC Planning COE Technical Manager II, ensuring project documentation, including solution designs, process flows, and user manuals. JIRA work: ensure tasks, stories, epics, defects, and spike assigned to you are well kept and maintained with weekly reports out though the JIRA tool Follow up the guidelines of the leaders of the GSC Planning COE team Qualifications Required: Education: Bachelor s degree in supply chain management, Business Administration, Engineering, Computer Science. Advanced degree is a plus. Experience: Minimum of 7-10 years of experience in supply chain management, with at least 5 years specializing in Kinaxis Rapid Response. Technical Skills: Proficiency in Kinaxis Rapid Response configuration, scripting, and integration. Strong understanding of supply chain planning and optimization principles. Project Management: Proven track record of leading and managing complex implementation projects, with a strong emphasis on meeting deadlines and delivering results. Analytical Skills: Strong problem-solving and analytical skills, with the ability to translate business requirements into effective solutions. Communication: Excellent verbal and written communication skills. Ability to present complex information clearly to both technical and non-technical stakeholders. Interpersonal Skills: Strong interpersonal and relationship-building skills. Ability to work effectively in a team environment and independently. Certifications: Kinaxis Rapid Response certification as Consultant and Master Preferred qualifications: Master s degree in business, supply chain, IS, statistics, mathematics, economics or related field. APICS certification Experience in the medical device or life sciences industry. Quality System Requirements: In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the BSC Quality Policy. Establishes and promotes a work environment that supports the Quality Policy and Quality System. Requisition ID: 589867 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Location(s): India-Maharashtra, Pune Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Accountable for delivering reliable, innovative, software medical device applications for our products. Significantly impact the software development of truly life changing patient therapies for the relief of debilitating diseases. Key Responsibilities: Server-side experience in Azure and .Net is must and should have experience in scaling Azure and .Net applications. C# Microsoft development using the .NET Framework - at least 5 years, Micro architecture Web Service delivery MS Service Fabric experience - Nice to have. Understanding fundamental design principles behind a scalable application. Solid understanding of Object-Oriented Analysis and Design. Familiarity with software configuration management and/or source code version control systems. (VS, Git) Experience with healthcare IT and/or software preferred. Used Agile methodology for software development process. Academics Qualifications Experience: Degree in Computer Science/Engineering or equivalent work experience. 8 years of software development experience Experience in any of the following areas is desired C# Net Azure MVC For Front End Strong Backend Server-Side Experience Required Microsoft Service - Kubernetes Service Fabrication From Microsoft (Good To Have) Web Service Delivery (Good To Have) Understanding fundamental design principles behind a scalable application. Solid understanding of Object-Oriented Analysis and Design. Familiarity with software configuration management and/or source code version control systems. Experience with healthcare IT and/or software preferred. Strong critical thinking and problem-solving skills. Demonstrated ability to work well in agile, small-team environments. Strong interpersonal and collaborative skills. Self-motivated and able to work autonomously when necessary. Must be eager to work with other dedicated programmers, including working in a remote development organization with co-workers in different geographic locations. Requisition ID: 588634 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you! At Boston Scientific, we recognize that nurturing a diverse and inclusive workplace helps us be more innovative and it is important in our work of advancing science for life and improving patient health. That is why we stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer. Boston Scientific maintains a prohibited substance free workplace. Pursuant to Va. Code 2.2-4312 (2000), Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination. Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company s policies or protocols change with regard to COVID-19 vaccination.

Additional Locations: India-Maharashtra, Pune Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Purpose The Kinaxis Maestro Developer needs to have expertise in end-to-end supply chain planning and a strong programming experience in RSL (Rapid Scripting Language), Java, and JavaScript. This role will play a key part in developing, enhancing, and supporting Kinaxis Maestro applications that optimize Boston Scientific s Global Supply Chain Planning processes. The ideal candidate will have a deep understanding of End-to-End Supply Chain operations and a proven track record of delivering scalable and efficient solutions. Additionally, this position will require supporting the development of UDP solutions for integrating, managing, and analyzing data across different systems and sources. Key Responsibilities Design, develop, and implement Supply Chain Planning solutions within the Kinaxis Maestro platform. Work closely with the Boston Scientific s Global Supply Chain Planning Business Analysts, Workstream Subject Matter Experts, Maestro s Consultants, and Maestro s Solution Architects to understand business requirements and translate these into practical technical solutions. Write clean, efficient, and well-documented code using RSL, Java, and/or JavaScript. Optimize and enhance existing Kinaxis applications and workflows to improve performance, ensure scalability and improve end user experience. Collaborate with cross-functional teams to ensure successful project delivery and integration with other enterprise systems such as SAP R3 ECC, SAP S4 HANA, among others. Troubleshoot and resolve technical issues related to Kinaxis Maestro applications. Provide technical guidance and mentorship to prospect developers and other team members as needed. Support implementation efforts in the development, configuration, customization, integration, and testing of Maestro s solutions. Design, develop, and maintain a Unified Data Platform to integrate diverse data sources across Boston Scientific s Global Supply Chain analytics Implement and maintain API integrations for data ingestion from external sources and API for sharing data with external systems Maintain accurate and detailed records of tasks, stories, epics, defects, and spikes in JIRA. Participate on the Sprint planning session to commit JIRA items for the following quarter. Adhere to the guidelines set by the Directors and Managers of the GSC Planning COE team and support their initiatives, and actively contribute to team goals and objectives. Stay updated with the latest developments in Kinaxis solutions and supply chain technologies and cloud platforms. Qualifications Required Bachelors degree: Computer Science, Information Technology, or a related field. Work Experience: +3 years of hands-on experience working with Kinaxis Maestro, including end-to-end Supply Chain Planning processes. Coding experience: Strong proficiency in RSL (Rapid Scripting Language), experience with Java, JavaScript, and SQL; for developing customized solutions and integrations. Cloud Platforms: Experience in AWS or Azure and data storage technologies such as Snowflake Supply Chain Planning: Solid understanding of Supply Chain Planning processes such as Demand Planning, Supply Planning, and Inventory optimization. ERP Systems : Knowledge of ERP systems (e.g., SAP, Oracle) and their integration with Kinaxis Maestro Analytical Skills: Excellent problem-solving skills and the ability to troubleshoot complex technical issues. Communication Skills: Strong collaboration and communication skills. Kinaxis certification: Authoring 1, Authoring 2, and Certified Integration Developer Preferred Qualifications Kinaxis : Additional certifications are a plus Cloud certifications: AWS or Azure Data Engineer Associate Other : Familiarity with cloud-based solutions and integrations (e.g., APIs). Quality System Requirements In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the BSC Quality Policy. Establishes and promotes a work environment that supports the Quality Policy and Quality System. Requisition ID: 589872 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Maharashtra, Pune Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Purpose Statement: We are seeking a highly skilled and experienced Software Verification Engineer III to join our team. The ideal candidate will have a strong background in testing medical software and test automation using Python. You will be responsible for analyzing requirements, writing test cases and test scenarios, transforming requirements into test protocols and automated test scripts, and setting up test stations. You will collaborate closely with development, requirements, and firmware teams, and provide regular status reports. Proficiency in using multiple version control, defect tracking, and peer review tools including Accurev, Bitbucket, JIRA, and Windchill is essential. Key Responsibilities: Analyze requirements and write comprehensive test cases and test scenarios. Transform requirements into detailed test protocols and automated test scripts for end-to-end evaluation. Conduct exploratory testing to identify potential issues and ensure software quality. Debug test failures and work with development teams to resolve issues. Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Understanding human anatomy and physiology and be able to apply that knowledge to the usage of medical devices. Set up, maintain test stations and debug infrastructure issues. Collaborate with development, requirements, and firmware teams to ensure seamless integration and testing processes. Provide regular status reports on testing activities and progress. Utilize multiple version control, defect tracking, and peer review tools including Accurev, Bitbucket, JIRA, and Windchill. Work with Linux-based systems such as Ubuntu for testing and automation tasks. Mentor team members on product features and functionality, test frameworks, protocol design. Qualifications: Functional Knowledge: Degree in Biomedical (preferred)/Any Engineering stream. 7+ years of experience in testing medical software. Extensive hands-on experience with Python frameworks and test automation using Python. Sound knowledge and experience with automation of GUI applications. Solid understanding of Object-Oriented Programming. Self-motivated and able to work autonomously when necessary. Strong ability to analyze requirements and write detailed test cases and test scenarios. Excellent collaboration skills with the ability to work effectively with various teams spread across geographical locations. Proficiency in using version control, defect tracking, and peer review tools including Accurev, JIRA, and Windchill. Experience with Linux-based systems such as Ubuntu. Experience with Squish testing tool. Requisition ID: 601338 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. About Role: Responsible for overall management of RD warehouse operations across Gurgaon and Pune, ensuring compliance with local quality and regulatory standards. Oversees inbound and outbound shipments, documentation, and coordination with global teams, customs, legal, and finance for import/export activities. Leads audits, warehouse security, staff training, and operational improvements while optimizing processes for efficiency. Manages budget, inventory automation, and warehouse staff performance to drive seamless supply chain operations. Role Responsibilities Overall management of RD warehouse operation, in Gurgaon and Pune facility, and ensure that they are complying required local quality and regulatory requirements. Overall management of RD storage beyond the warehouse. Close monitoring of inbound and outbound shipment from warehouse ensures all documentation trail is in place. Training to Warehouse staff related to warehouse SOP and WI. Co-ordination with Global teams, CHA, Reg Affairs, Legal, and finance related to import and export product relate shipments and troubleshoot situations. Co-ordination with CHA for timely clearance of shipment and provide them necessary information if required for custom clearance. Co-ordination with finance team for timely duty payment for custom clearance and payment of others vendor. Handle various type of Audit - Quality Audit by local and global teams, Statutory Audit by 3rd party auditors, and unannounced CDSCO audits. Complies with state, and local warehousing, material handling, and shipping requirements; Enforcing adherence to requirements; advising management on needed actions. Safeguards warehouse operations and contents by establishing and monitoring security procedures and protocols. Maintains physical condition of warehouse by planning and implementing new design layouts; inspecting equipment; issuing work orders for repair and requisitions for replacement. Achieves financial objectives by preparing an annual budget; scheduling expenditures; analyzing variances; initiating corrective actions. Maintains warehouse staff by recruiting, selecting, orienting, and training employees. Maintains warehouse staff job results by coaching, counseling, and disciplining employees, planning, monitoring, and appraising job results. Adhere to all warehousing, handling and shipping legislation requirements coordinate and monitor the receipt, order, assembly and dispatch of goods Role Requirements Graduate degree. MBA will be preferred. At least 10-15 years of relevant experience in warehouse management and progressive experience in Supply Chain / Operations management. Exposure to and experience working in regional/global supply chain operations. Has a proven track record of managing multiple tasks within a matrix working environment and simplifying that matrix for stakeholders and team. Strong process, project and time management skills with the ability to organize and handle multiple priorities. Working experience with warehouse inventory management and automation. Excellent communication skills. Proactive, enjoys working in a challenging environment, results-oriented and a team player. Requisition ID: 600921 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. About Role: Provides mechanical engineering support for developing innovative medical devices, ensuring designs meet customer and business needs. Applies principles of engineering, physics, and material science to optimize and evaluate mechanical and electro-mechanical components. Manages design risks, collaborates with internal and external teams, and ensures robust documentation and compliance with quality systems. Proficient in CAD design, GDT, material sciences, and statistical analysis, with a strong focus on process improvement and technical communication. Key Responsibilities: Responsible for providing mechanical engineering support in the creation and the development of new medical device products (invasive and non-invasive). Key Responsibilities Apply principles of Mechanical engineering, Physics, and Material Science to perform data driven development, optimization, and evaluation of novel or iterative designs of mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment, based on customer and business needs. Defines and implements specifications, inputs/outputs, working parameters, and test methods using current best practice engineering methods and technologies. Assesses design risks and mitigations through tools such as FMEA, Fault tree, etc. Works closely with key internal and external specialty resources to ensure to ensure robust holistic device / component design and to address complex design issues. Continuously improves process and work methodologies by interfacing with peers/cross-functional groups and analyzing activities to improve workflow and work processes. Provides clear communication to stakeholders for key technical updates. Creates robust documentation of requirements, protocols, evaluations, reports, etc. throughout all phases of research and development by writing clear and concise documents. Complies with site and department specific procedures on record keeping, use of log books, materials receiving, and inventory control. Completes time records and reports projects allocated time. Adheres to all EHS procedures and general housekeeping SOPs. Remains knowledgeable of technologies within functional area. Writes and submits intellectual property (patents). Reviews or coordinates vendor activities to support development. Contributes to a strong team culture around high expectations and high performance and Experience Qualifications and Skill-Set BE/B.Tech degree in Mechanical/ Biomedical Engineering. Minimum 3 years of RD / NPD experience, preferably in medical devices. Knowledge in medical grade material sciences and processing - Metals, Polymers Proficient in CAD Design, GDT, Tolerance stack-ups Knowledge of quality system processes that need to be applied for product development. Basic stats knowledge Requisition ID: 602001 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

We are looking for a software engineer with a strong software development experience in User Interface (UI) development using Qt to join our exciting and fast-paced development team. A successful candidate who joins us, will be involved in all aspects of the systems software, including user interfaces. They will also interface with other teams, such as systems engineering, hardware engineering and technicians from the field, to develop meaningful tools for the Opal Mapping System. T he Opal Mapping System centers around a real-time virtual world of the human heart. As a physician probes the heart with a catheter, the system generates an accurate anatomical model of the chamber. High-performance rendering and algorithmic techniques are vital to creating a stunning view and providing the physician with instant feedback. Our tools include C++, OpenGL, GLSL, OpenCL, Qt, and Linux. Key Responsibilities: Design, develop and maintain user interfaces for our medical device using Qt. Provide technical leadership to the team in software design and best in class software development methodologies and practices. Solve difficult problems and always strive to make things better and achieve engineering excellence. Partner with other teams including marketing, systems engineering, QA, hardware and regulatory to understand requirements and bring the best solutions forward. Requirements: BTech/MTech in Computer Science/Electrical engineering or equivalent experience, with a strong software development background. 10 - 14 years of experience with having delivered successful mission critical products. Expertise in C++, Qt and familiarity with one other scientific computing/scripting language such as Python or MATLAB. Working knowledge in Unix. Strong in solving complex problems and demonstrated ability to adapt, proactive and a positive influence to the rest of the team. Excellent communication skills with the ability to adapt to the target audience. Expertise in developing software using Scrum methodology. In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Preferred Qualifications: Strong experience with designing and implementing medical device software. Experience working with third-party C++ libraries such as STL, Qt, Boost. Experience developing systems with intuitive User Interfaces. Experience writing SW for embedded systems that interface with sensors.

We are looking for a software engineer with a strong software development experience in User Interface (UI) development using Qt to join our exciting and fast-paced development team. A successful candidate who joins us, will be involved in all aspects of the systems software, including user interfaces. They will also interface with other teams, such as systems engineering, hardware engineering and technicians from the field, to develop meaningful tools for the Opal Mapping System. T he Opal Mapping System centers around a real-time virtual world of the human heart. As a physician probes the heart with a catheter, the system generates an accurate anatomical model of the chamber. High-performance rendering and algorithmic techniques are vital to creating a stunning view and providing the physician with instant feedback. Our tools include C++, OpenGL, GLSL, OpenCL, Qt, and Linux. Key Responsibilities: Design, develop and maintain user interfaces for our medical device using Qt. Provide technical leadership to the team in software design and best in class software development methodologies and practices. Solve difficult problems and always strive to make things better and achieve engineering excellence. Partner with other teams including marketing, systems engineering, QA, hardware and regulatory to understand requirements and bring the best solutions forward. Requirements: BTech/MTech in Computer Science/Electrical engineering or equivalent experience, with a strong software development background. 15+ years of experience with having delivered successful mission critical products. Expertise in C++, Qt and familiarity with one other scientific computing/scripting language such as Python or MATLAB. Working knowledge in Unix. Strong in solving complex problems and demonstrated ability to adapt, proactive and a positive influence to the rest of the team. Excellent communication skills with the ability to adapt to the target audience. Expertise in developing software using Scrum methodology. In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Preferred Qualifications: Strong experience with designing and implementing medical device software. Experience working with third-party C++ libraries such as STL, Qt, Boost. Experience developing systems with intuitive User Interfaces. Experience writing SW for embedded systems that interface with sensors.

Additional Locations: India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Responsible for providing mechanical engineering support in the maintenance of project DHF deliverables in Requirements Management (RM) tool for new and sustaining medical device products (invasive and non-invasive). Key Responsibilities: Read and interpret technical drawings, procedures, and protocols. Import and maintains the project documentation in online RM tool throughout all phases of NPD and Sustaining. Investigates and evaluates the compliance requirements driven from organization s QMS/Work Instructions and validate the same in templates developed in RM tool. Investigates and evaluates existing RM tools/technologies - JAMA, Polarion etc. Investigates compliance gaps in project documents and resolve them with project stake holders. Collaborate with cross-functional process, method, and teams to understand and implement solutions to resolve compliance gap issues in documents. Performs validation of patches and versions of RM tool as and when available. Support multiple projects across different time zones - Asia, Ireland, and North America Qualifications: Mechanical Engineering ( B. E. /B. Tech) with 8-10 years of experience. Preferred experience in management of DHF documentation during full life cycle of medical device as per ISO 13485, and ISO 14971 Preferred experience in RM tools like JAMA, Polarion, DOORS, Cockpit. Knowledge of MS Office Tools - Word, Excel, PowerPoint. Strong attention to detail with good communication skills. Strong strategic / analytical thinking and problem-solving abilities, with a data-driven approach to decision-making. Ability to collaborate and work as a team player. Nice to have experience in product lifecycle management software and tools. Willingness to work in an agile environment. Requisition ID: 596291 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Purpose Statement: Primary focus is providing moderately complex administrative support for individuals and/or department. Works under general supervision and receives detailed instructions only for new assignments. Key Responsibilities: Performs general administrative duties that may include photocopying, coordinating meetings/appointments, typing, faxing, ordering/maintaining supplies, arranging travel, preparing and/or sorting mail. Serves as a point of contact for stakeholders.Contacts are typically with individuals within own organization and occasionally with contacts outside own organization and involve obtaining or providing information requiring some explanation or interpretation. Answers questions related to established policies and procedures. Directs people to the appropriate resource. Leadership travel arrangements and co-ordination with the travel desk Arranging team dinners, monthly meetings, booking conference rooms etc. Travel Food arrangements for visitors as instructed by leadership. Managing outlook calendars, schedules for executives. Contributing actively into all site ERGs and events. Receives, check and arranges documents for approval and records. Maintains tracker and works cross functionally to ensure compliance and process integrity. Makes decisions within established guidelines regarding planning, organizing, and scheduling of work. Creates and types of routine documents (letters/memos/e-mails, presentations, etc.) and revises as necessary; ensures accuracy in grammar and spelling. Manages work in a confidential manner, ensuring information is shared with internal and external individuals in an appropriate manner. Confidential information typically consists of department or employee sensitive information (i.e. employee salaries). Achievement of Boston Scientific Quality goals and do the mandatory e-learning courses. Ensures awareness and compliance with applicable standard operating procedures to meet, comply and champion all quality and regulatory commitments of Boston Scientific. Quality System Requirements: In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Job Scope and Leveling Guidelines: Functional Knowledge: Requires expanded conceptual and technical and/or functional knowledge in own job function. Essential Skill set to perform the job- Proficiency in Microsoft office- Excel, PowerPoint and Word. Proficiency in spoken and written English. Business Expertise: Demonstrates working knowledge of business and industry practices and company processes to accomplish own work. Leadership: No supervisory responsibility; accountable for own contributions and meeting objectives. Problem Solving: Uses and exercises judgment to solve problems in straightforward situations and determine appropriate action/solutions. Works under general direction from more senior level roles/manager. Impact: Impacts quality of own work and the work of others on the team; works within guidelines and policies. Interactions (and Communications): Explains factual information of limited complexity to others in straightforward situations Organizes, presents and explains data/ information, primarily to internal audiences Requisition ID: 603170 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Maharashtra, Pune Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Purpose Statement: We are seeking a highly skilled and experienced Software Verification Engineer III to join our team. The ideal candidate will have a strong background in testing medical software and test automation using Python. You will be responsible for analyzing requirements, writing test cases and test scenarios, transforming requirements into test protocols and automated test scripts, and setting up test stations. You will collaborate closely with development, requirements, and firmware teams, and provide regular status reports. Proficiency in using multiple version control, defect tracking, and peer review tools including Accurev, JIRA, and Windchill is essential . Key Responsibilities: Analyze requirements and write comprehensive test cases and test scenarios. Transform requirements into detailed test protocols and automated test scripts for end-to-end evaluation. Conduct exploratory testing to identify potential issues and ensure software quality. Debug test failures and work with development teams to resolve issues. Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Understanding human anatomy and physiology and be able to apply that knowledge to the usage of medical devices. Set up, maintain test stations and debug infrastructure issues. Collaborate with development, requirements, and firmware teams to ensure seamless integration and testing processes. Provide regular status reports on testing activities and progress. Utilize multiple version control, defect tracking, and peer review tools including Accurev, JIRA, and Windchill. Work with Unix-based systems such as Ubuntu for testing and automation tasks. Mentor team members on product features and functionality, test frameworks, protocol design. Requirements: Degree in Biomedical (preferred)/Any Engineering stream. 7+ years of experience in testing medical software. Extensive hands-on experience with Python frameworks and test automation using Python. Sound knowledge and experience with automation of GUI applications. Solid understanding of Object-Oriented Programming. Self-motivated and able to work autonomously when necessary. Strong ability to analyze requirements and write detailed test cases and test scenarios. Excellent collaboration skills with the ability to work effectively with various teams spread across geographical locations. Proficiency in using version control, defect tracking, and peer review tools including Accurev, JIRA, and Windchill. Experience with Unix-based systems such as Ubuntu Requisition ID: 603260 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Purpose Statement: Develops, establishes, and maintains quality engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, communication on quality initiative. Key Responsibilities: Be a part of core project team and lead the quality engineering across the entire development cycle. Support the development of CTQ s, design input and output documents. Support the fixture qualification and test method validation. Support the development and implementation of design verification and validation plans with project design lead. Support product risk management, usability, reliability and design validation efforts for new product development and design change projects. Participate and implement tools like Design of Experiments (DOE s), FMEA sessions, Risk Management and ensure compliance to CTQ s and safety requirements. Responsible for co-leading stage gate reviews and signatory on all PDP document approvals Manage electronic document control and version control on all project related documents. Ensure adherence to the quality systems and design assurance SOPs and Boston Scientific s PLCP. Support usability, reliability, testing, verification and validation testing - internal and local vendors. Provide statistical testing and reliability plans. Work closely with regulatory team to drive alignment of project documentation and regulatory requirements. Provide quality and regulatory compliance guidance as needed to product development or design change project teams to assure country specific compliance to the laws and regulations of the targeted market for distribution. Ensure appropriate Project/Sustaining Quality Deliverables are created and properly executed (e. g. Project Design & Development Plan, Risk Management Plan, Hazard Analysis, Use and Design FMEA, Field Assessment Plan, and Software Validation Plan if applic Co-Lead CAPA efforts, and apply sound, systematic problem-solving methodologies identifying, prioritizing, communicating, and driving resolution of quality issues (e. g. , 5 why s analysis, Is-Is Not analysis, and Six Sigma problem solving methodologies). Devise and support the implementation of effective quality assurance, process controls, statistical analyses, and metrics that assure products meet or exceed internal quality as well as statutory requirements. Participate in ISO13485 site certification for the R&D center. Requirements: Bachelors (or higher) degree in engineering with preference mechanical engineering. 5-7+ years of experience in medical device R&D quality engineering, systems and / or quality engineering supporting R&D projects, design assurance and documentation. Professional training and certification in in Quality Management Systems including ISO 13485, Risk management ISO 14971, design assurance / control, verification and validation. Sound understanding of medical device regulatory requirements for Class II and III medical devices. Project planning - resourcing, timelines, quality and budgets. Skilled in implementing Quality tools like design of six sigma, risk management, FMEA, FTA (Fault Tree Analysis). Preference for candidates with CQE certification or similar training and experience Proficient in project management tools like MS project. Experience in GD&T Well versed with statistical analytical techniques and s/w tools like MATLAB, MINITAB. Requisition ID: 601995 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Purpose Statement: Serves as a Supplier Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional and corporate quality goals and priorities. Provides focused Supplier quality engineering support within new product development, operational, or system/services support. Drives improvement and corrective action in the quality of components sourced from outside suppliers. Provides technical support in the selection of suppliers. Develops acceptance criteria for materials. Monitors supplier performance to drive supplier corrective action, manufacturing yield issues and field failures. Key Responsibilities: Plans and conducts scheduled assessments of suppliers to assess compliance with Boston Scientific requirements, includes assessment preparation meetings and scheduling in advance of site visit, conducts and confirms follow-up actions on Supplier Quality System Assessments. 8-10 years of relevant experience. Assesses supplier capabilities through direct visits, technical discussions and Quality System Assessments. Prepares detailed trip reports and Assessment Reports to document assessment findings and observations. Communicates quality issues to suppliers as needed and provides assistance to develop corrective actions. Participates with Corporate and regional Supplier Quality organization on policy/procedure/ guideline development, includes incorporation of this information into corporate and divisional programs through document reviews, protocol reviews, validation reviews, and training programs. Works with various partners to assess and address material quality issues. Tracks and trends supplier performance, taking remedial action as needed. Interfaces with the Procurement and Sourcing Specialists. Assist suppliers in formation of statistical sampling plans, inspection methodology, and quality procedures. Maintains accuracy of ERP Vendor Assessment Report and Supplier Profile Reports. Ensure adherence to the quality systems, supplier and internal audit SOPs and Boston Scientific s PLCP. Partners with BSC material suppliers to ensure appropriate application of process validation, process control, and risk management; and the investigation/correction of process failures when needed. Develop, interpret and implement appropriate process monitoring and control methods consistent with the level of process/product risk. Collect data and execute/conduct various analytical/statistical analysis and interpretation as part of Supplier improvements. Develop, interpret and implement standard and non-standard sampling plans. Handling and leading SCAR s, NCEP, CAPA and other audit outcomes. Handling of product recall related activities to suppliers. Actively participation and leading activities assigned to SQE. Requisition ID: 602704 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Purpose Statement: Provide Software Quality Assurance support, to corporate software policies and regulations, at the Penang site. Provides support on software validation requirements to project teams that are implementing software systems and provides an independent review to teams. Key Responsibilities: Develop an in-depth knowledge of BSC s policies and procedures, especially those that apply to BSC's software. Understand and be able to explain how these policies achieve compliance with appropriate regulations and standards. Be able to interpret policies and regulations in support of a wide variety of software such as Custom, Off-The-Shelf, as well as everything from equipment controllers to database-driven solutions. Apply these policies and procedures to the site s software systems and computer-driven equipment. Be able to explain software validation deliverables to business owners of the applications. Ability to perform risk analysis on multiple systems. Create validation documentation for a wide range of software applications including equipment software. Provide guidance and direction on the acceptability of Software Quality deliverables, based on requirements and templates given. Requirements: Bachelors (or higher) degree in engineering with preference Computer Science. 5-7+ years of experience in medical device R&D quality engineering, systems and / or quality engineering supporting R&D projects, design assurance and documentation. Professional training and certification in in Quality Management Systems including ISO 13485, Risk management ISO 14971, design assurance / control, verification and validation. Sound understanding of medical device regulatory requirements for Class II and III medical devices. Project planning - resourcing, timelines, quality and budgets. Skilled in implementing Quality tools like design of six sigma, risk management, FMEA, FTA (Fault Tree Analysis). Preference for candidates with CQE certification or similar training and experience Proficient in project management tools like MS project. Experience in ISO 62304 Requisition ID: 601996 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: India-Haryana, Gurgaon Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. Purpose Statement: Responsible for providing Quality Engineering Input to support Manufacturing, Manufacturing Engineering, and R&D activities that involve the development or use of software products. Key Responsibilities: Develops, applies, revises, and maintains quality standards for software products that the company develops as part of finished products or in support of manufacturing, manufacturing engineering, or quality processes. Actively participates in New Product Development, Design Review, and Design Control Activities, as related to software products. Develops and implements Process and Product Software Verification and Validation activities with reference to external standards and regulations, such as FDA, ISO, IEEE. Leads the activities associated with the Software products risk assessment. Provides technical guidance and training to other Department members in Software QA Engineering areas of expertise. Controls and maintains the database for tracking defects associated with the products during the design life cycle. Provides input to, defines and approves Product and Process Validations and Reports. Establishes requirements for Installation and Operational Qualifications for new and replacement equipment. Requirements: Bachelors (or higher) degree in engineering with preference Computer Science. 9+ years of experience in medical device R&D quality engineering, systems and / or quality engineering supporting R&D projects, design assurance and documentation. Professional training and certification in in Quality Management Systems including ISO 13485, Risk management ISO 14971, design assurance / control, verification and validation. Sound understanding of medical device regulatory requirements for Class II and III medical devices. Project planning - resourcing, timelines, quality and budgets. Skilled in implementing Quality tools like design of six sigma, risk management, FMEA, FTA (Fault Tree Analysis). Preference for candidates with CQE certification or similar training and experience Proficient in project management tools like MS project. Experience in ISO 62304 Requisition ID: 602955 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we ll give you the opportunity to harness all that s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we ll help you in advancing your skills and career. Here, you ll be supported in progressing - whatever your ambitions. About the Role: The Customer Care department is crucial in managing and administering the order management of medical equipment and processing orders and inquiries. You will join a dynamic international team supporting local Growth and Emerging Markets and global distributors in fulfilling product orders. Your role will involve managing order handling and ensuring an exceptional customer experience. Location:- Gurugram, Haryana Key Responsibilities Performing order entry or order management functions with high quality and delivering expected performance with the needed productivity. Utilizing your expertise in the German language to support the team by interpreting customer comments on faxes and aligning them with process knowledge to solve queries. Meeting all required metrics such as average handling time, quality targets, etc. , as assigned per the process guidelines. Aligning with all queries shared by the local customer care team and providing resolutions based on information given by customers. Being efficient with MS Excel, PowerPoint, MS Word, and MS Outlook Teams. Creating required reports and presentations. Applying basic conceptual knowledge of theories, practices, and procedures within the job function. Performing assignments using existing procedures. Receiving guidance and direction from more senior-level roles/managers within the job function. Applying general business knowledge obtained through education or past experience with guidance from others. No supervisory responsibility; accountable for own contributions and meeting objectives with guidance from more senior-level roles/managers. Working within standardized procedures and practices to achieve objectives and meet deadlines. Exchanging straightforward information, asking questions, and checking for understanding. Compiling and organizing data/information to support discussions and inform decision-making. Requirements Minimum education level: University (Bachelor s Degree) Minimum 4-5 years of experience in Customer Service and working with order-to-cash processes, ideally in the Medical Devices/Medical Technology sector (or similarly regulated industry, e. g. , Pharmaceuticals, etc. ) Experience with and proficiency using SAP and the Microsoft Office suite of products (Excel, PowerPoint, Outlook) Excellent interpersonal and communication skills with a customer-centric mindset Highly organized Ability to manage a complex workload in a matrixed environment Willingness to learn, grow, and develop Business fluency in English - written and verbal is non-negotiable Proficiency in German language Requisition ID: 603370 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn t just business, it s personal. And if you re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!

Purpose As a Principal Solutions Rapid Response Consultant GSC Planning COE, you will play a critical role in guiding our Center of Excellence team and the different teams of Global Supply Chain Planning through the implementation and optimization of Kinaxis Rapid Response solutions. You will leverage your expertise in supply chain management and Kinaxis technology to deliver high-quality consulting services that drive tangible business results in the form of quickly designing and implementing technology solutions to address immediate and urgent business needs. Their primary goal is to ensure Boston s Scientific Rapid Response technology infrastructure what can adapt to sudden changes, emergencies, or critical demands. Key Responsibilities Work closely with business users to understand their requirements, challenges, and objectives. Develop strong relationships to become a trusted advisor. Design and architect Kinaxis Rapid Response solutions tailored to meet the specific needs of Boston s Scientific. Ensure solutions are scalable, sustainable, and aligned with best practices. Lead and manage the implementation of Rapid Response solutions, including configuration, customization, integration, and testing. Oversee project timelines, resources, and budgets with the Senior GSC Planning COE Technical Manager II to ensure successful delivery. Provide comprehensive training to users on Rapid Response functionality and best practices. Offer ongoing support and troubleshooting to ensure optimal use of the platform. Stay up-to-date with the latest Kinaxis Rapid Response features and industry trends. Identify opportunities for cusers to enhance their supply chain processes and achieve greater efficiencies. Collaborate with internal teams, including GSC Planning COE workstream leaders and business analysts, product development, and business users, to ensure seamless project execution Follow up and use, implement, and maintain the guidelines of documentation as stated by the Senior GSC Planning COE Technical Manager II, ensuring project documentation, including solution designs, process flows, and user manuals. JIRA work: ensure tasks, stories, epics, defects, and spike assigned to you are well kept and maintained with weekly reports out though the JIRA tool Follow up the guidelines of the leaders of the GSC Planning COE team Qualifications Required: Education: Bachelor s degree in supply chain management, Business Administration, Engineering, Computer Science. Advanced degree is a plus. Experience: Minimum of 7-10 years of experience in supply chain management, with at least 5 years specializing in Kinaxis Rapid Response. Technical Skills: Proficiency in Kinaxis Rapid Response configuration, scripting, and integration. Strong understanding of supply chain planning and optimization principles. Project Management: Proven track record of leading and managing complex implementation projects, with a strong emphasis on meeting deadlines and delivering results. Analytical Skills: Strong problem-solving and analytical skills, with the ability to translate business requirements into effective solutions. Communication: Excellent verbal and written communication skills. Ability to present complex information clearly to both technical and non-technical stakeholders. Interpersonal Skills: Strong interpersonal and relationship-building skills. Ability to work effectively in a team environment and independently. Certifications: Kinaxis Rapid Response certification as Consultant and Master Preferred qualifications: Master s degree in business, supply chain, IS, statistics, mathematics, economics or related field. APICS certification Experience in the medical device or life sciences industry. Quality System Requirements: In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the BSC Quality Policy. Establishes and promotes a work environment that supports the Quality Policy and Quality System.

PURPOSE STATEMENT Design, develop and test software applications for medical software products or other software related products for implantable medical device products for R&D Division at Boston Scientific. Independently conducts the work as part of a major research and/or development project. Can provide technical direction/review on broad scope or complex projects. Viewed as an expert in one or more in-house technologies. KEY RESPONSIBILITIES Responsible for developing software and/or testing implantable neural stimulation systems or other software related products. Provide competitive advantage in performance, cost and quality. Work on C# applications using technology such as WPF, UWP, SOA (Service Oriented Architecture), and Entity framework Follow the full design life cycle process including driving efforts in requirements specification, design activities, planning, code reviews and creating corresponding artifacts. Provide complete expert engineering solutions to impactful and high-visibility initiatives and projects. Lead and mentor a team of talented Software Engineers. Promote a collaborative environment and pragmatic engineering decision-making. Build collaborative relationships with key leaders and peers, internally and externally, across the organization. KEY SKILLS Strong oral and written communication skills Demonstrated experience in software development lifecycle (Agile), object-oriented design methodology Experience with medical device regulatory guidance such as 21 CFR Part 820, IEC 62304 and ISO 13485 Preferred experience with software configuration tools for source code control (Git), issue tracking (Jira), requirements management (Cockpit), code review tools (Code Collaborator) and 3rd party project build tools ( Demonstrated technical leadership skills Creative / innovative thinker Good organizational and multi-tasking skills Bachelors degree in computer science, electrical engineering, or a related field 10+ years of software development with fluency coding in multiple programming languages, such as C# / .NET Preferred familiarity with Brainlab Surgical Planning Software QUALITY SYSTEM REQUIREMENTS In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. For those individuals that supervise others, the following statements are applicable: Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the BSC Quality Policy. Establishes and promotes a work environment that supports the Quality Policy and Quality System. JOB SCOPE AND LEVELING GUIDELINES Functional Knowledge Requires specialized and comprehensive technical and/or functional knowledge in own job function or field and has full understanding of other related job functions Leverages this knowledge to recommend new and/or improved work processes, typically at an area level impacting various teams Business Expertise Applies knowledge of business and industry best practices and how own area integrates with others to achieve objectives to drive results Is aware of the competition and the factors that differentiate them in the market Leadership Acts as a resource and mentor for colleagues with less experience May lead projects with manageable risks and resource requirements, often broader, cross-functional projects Problem Solving Solves complex and diverse problems, takes a new perspective on existing solutions and exercises judgment based on the analysis of multiple sources of information using specialized knowledge of various alternatives and their impact on the business Works independently within broad guidelines and policies, receives minimal guidance Impact Impacts the ongoing achievement of customer, operational, project/program or key business/organizational/service objectives and recommends improvements within area of responsibility Interactions (and Communications) Explains difficult or sensitive information to facilitate productive discussion; works to build consensus Regularly leads discussions and makes presentations in cross-functional meetings, effectively presenting information to explain recommendations and implications

Purpose Statement Boston Scientific is seeking an experienced Principal Cybersecurity Engineer with a strong background in the design, development, and testing of cybersecurity features and controls in a regulated industry. This individual will be responsible for overseeing and guiding the cybersecurity strategy throughout the product lifecycle, ensuring compliance with relevant standards and regulations within the R&D Division. KEY RESPONSIBILITIES Responsible for leading the design, implementation, and maintenance of comprehensive security measures across all stages of medical device development, ensuring compliance with relevant regulations and standards while protecting patient data and device integrity Lead the design and implementation of secure architectures for new medical devices, considering connectivity, data protection, access controls, and secure communication protocols Conduct thorough vulnerability assessments and penetration testing on medical devices to identify potential security flaws and implement corrective actions Ensure compliance with relevant medical device cybersecurity regulations and standards, including documentation and reporting requirements. Mentor and guide junior cybersecurity engineers on best practices, security techniques, and emerging threats within the medical device domain Collaborate with cross-functional teams including product development, quality assurance, regulatory affairs, and clinical teams to address cybersecurity concerns KEY SKILLS AND QUALIFICATIONS Deep understanding of cybersecurity principles and concepts, including cryptography, network security, authentication, authorization, and data protection. Expertise in medical device cybersecurity standards and regulations (FDA, IEC 62304, ISO 14971, IEC 81001-5-1) Proven experience in threat modeling, risk assessment, and vulnerability management within the medical device context Strong knowledge of secure coding practices and software development methodologies Experience with penetration testing tools and techniques for medical devices Excellent communication and collaboration skills to work effectively with cross-functional teams Bachelors degree in computer science, electrical engineering, or a related field 10+ years of experience with cybersecurity and software systems Advanced cybersecurity certifications (e.g., CISSP, CISA, OSCP) are highly desirable QUALITY SYSTEM REQUIREMENTS In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. JOB SCOPE AND LEVELLING GUIDELINES Functional Knowledge Requires specialized and comprehensive technical and/or functional knowledge in own job function or field and has full understanding of other related job functions Leverages this knowledge to recommend new and/or improved work processes, typically at an area level impacting various teams Business Expertise Applies knowledge of business and industry best practices and how own area integrates with others to achieve objectives to drive results Is aware of the competition and the factors that differentiate them in the market Leadership Acts as a resource and mentor for colleagues with less experience May lead projects with manageable risks and resource requirements, often broader, cross-functional projects Problem Solving Solves complex and diverse problems, takes a new perspective on existing solutions and exercises judgment based on the analysis of multiple sources of information using specialized knowledge of various alternatives and their impact on the business Works independently within broad guidelines and policies, receives minimal guidance Impact Impacts the ongoing achievement of customer, operational, project/program or key business/organizational/service objectives and recommends improvements within area of responsibility Interactions (and Communications) Explains difficult or sensitive information to facilitate productive discussion; works to build consensus Regularly leads discussions and makes presentations in cross-functional meetings, effectively presenting information to explain recommendations and implications

Purpose Statement: We are seeking a highly skilled and experienced Software Verification Engineer III to join our team. The ideal candidate will have a strong background in testing medical software and test automation using Python. You will be responsible for analyzing requirements, writing test cases and test scenarios, transforming requirements into test protocols and automated test scripts, and setting up test stations. You will collaborate closely with development, requirements, and firmware teams, and provide regular status reports. Proficiency in using multiple version control, defect tracking, and peer review tools including Accurev, JIRA, and Windchill is essential . Key Responsibilities: Analyze requirements and write comprehensive test cases and test scenarios. Transform requirements into detailed test protocols and automated test scripts for end-to-end evaluation. Conduct exploratory testing to identify potential issues and ensure software quality. Debug test failures and work with development teams to resolve issues. Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Understanding human anatomy and physiology and be able to apply that knowledge to the usage of medical devices. Set up, maintain test stations and debug infrastructure issues. Collaborate with development, requirements, and firmware teams to ensure seamless integration and testing processes. Provide regular status reports on testing activities and progress. Utilize multiple version control, defect tracking, and peer review tools including Accurev, JIRA, and Windchill. Work with Unix-based systems such as Ubuntu for testing and automation tasks. Mentor team members on product features and functionality, test frameworks, protocol design. Requirements: Degree in Biomedical (preferred)/Any Engineering stream. 7+ years of experience in testing medical software. Extensive hands-on experience with Python frameworks and test automation using Python. Sound knowledge and experience with automation of GUI applications. Solid understanding of Object-Oriented Programming. Self-motivated and able to work autonomously when necessary. Strong ability to analyze requirements and write detailed test cases and test scenarios. Excellent collaboration skills with the ability to work effectively with various teams spread across geographical locations. Proficiency in using version control, defect tracking, and peer review tools including Accurev, JIRA, and Windchill. Experience with Unix-based systems such as Ubuntu

Purpose As a Senior Kinaxis Maestro Technical Consultant in the GSC Planning COE, you will be responsible for independently managing the implementation and optimization of authoring and solution development in Kinaxis Maestro. You will play a critical role in designing, configuring, and deploying advanced Global Supply Chain planning solutions within the Kinaxis Maestro platform. This position requires a deep understanding of Kinaxis authoring tools, data modeling, automations, and workflow configuration to meet complex business requirements. Key Responsibilities Authoring and Configuration: Design and implement custom solutions within the Kinaxis Maestro framework, including workflows, control tables, automations, and data models. Develop custom and support advanced supply chain planning scenarios. Configure and optimize what-if scenarios and simulations to support business decision-making. Data Integration and Management: Support the integration of Kinaxis Maestro with the ERP systems SAP ECC R3 and SAP S4 HANA and other data sources. Develop and maintain a streamlined ETL processes for importing/exporting data to and from Kinaxis Maestro for all solutions Solution Design and Implementation: Lead the design, development, and deployment of end-to-end supply chain planning solutions. Author custom dashboards and analytics for real-time supply chain monitoring and reporting. Performance Optimization: Troubleshoot and optimize workflows and dashboards for improved performance. Implement best practices for scalable and maintainable solutions. Collaboration and Stakeholder Engagement: Work closely with Solution Architects, Business Analysts, and IT teams to gather requirements and deliver tailored solutions. Provide technical leadership and mentorship to junior consultants or developers. Documentation and Governance: Maintain comprehensive documentation for all authored solutions, workflows, and configurations. Ensure compliance with organizational governance standards and best practices. Create and maintain comprehensive project documentation, including solution designs, process flows, and user manuals. Ensure all documentation is up-to-date and accessible as directed by the Sr GSC Planning COE Technical Manager II. Maintain accurate and detailed records of tasks, stories, epics, defects, and spikes in JIRA. Generate reports and communicate updates regularly and assist in preparing weekly reports and update your JIRA items at least once per week. Participate on the Sprint planning session to commit JIRA items for the following quarter. Adhere to the guidelines set by the Directors and Managers of the GSC Planning COE team and support their initiatives. and actively contribute to team goals and objectives. Stay up-to-date with Kinaxis Maestro Monitor Platform Developments and Stay up-to-date with the latest Kinaxis Rapid Response features and industry trends. Proactively suggest enhancements to supply chain processes. Qualifications Required Education: Bachelor s degree in supply chain management, Business Administration, Engineering, Computer Science, or a related field. Experience: 3-7 years of experience in supply chain management, with 4-6 years specializing in Authoring in Kinaxis Maestro. Technical Skills: Proficiency in Kinaxis Rapid Maestro configuration, authoring, and integration. Strong understanding of supply chain planning principles. Project Management: Experience in managing small to medium-sized projects with a focus on delivering results within defined timelines. Analytical Skills: Strong problem-solving and analytical skills. Ability to translate complex business requirements into effective technical solutions. Communication: Excellent verbal and written communication skills. Ability to present information clearly to both technical and non-technical stakeholders. Interpersonal Skills: Strong interpersonal skills with the ability to build and maintain relationships across various teams. Certifications: Kinaxis Maestro certification as Author-1 and Author-2 Preferred Qualifications Experience: Experience in the medical device or life sciences industry. Certifications: APICS certification or equivalent is preferred. Quality System Requirements In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures. Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the BSC Quality Policy. Establishes and promotes a work environment that supports the Quality Policy and Quality System.

The BSC Endosurgery Territory Manager will be responsible for driving sales revenue to exceed division priorities, defining and developing new business opportunities that clearly reflect the company s vision and priorities, and functioning in and contributing to overall team success. Individuals will exhibit strong clinical excellence, stay current on products, programs, and competitive knowledge, and be able to face up to program situations quickly, directly, and without hesitation. The candidate will have experience and be comfortable in the hospital and office-based settings and be creative in their problem-solving. The Territory Manager will develop key relationships through frequent and routine customer visits, product demonstrations, product in-services, and procedural observation. Relationships must be established with Physicians, Nurses, Technicians, Hospital Infection control, and Materials Management. Additionally, the candidate will build and maintain constructive strategic relationships in key accounts and be able to take actions that are consistent with the stated organizational goals. The candidate will manage their territory with integrity and in accordance with our Code of Conduct. Responsibilities and Requirement : Graduate with 3+ Years of experience in medical devices. Should have strong communicate skills Develops quarterly plans designed to achieve revenue targets. Clinical excellence in respective disease states. Build sustainable business relationships. Drive sales revenue to exceed division priorities. Define and develop new business opportunities that clearly reflect the companys vision and priorities. Build and maintain sustainable strategic relationships in key accounts. Stay current on BSC products / programs / competitive knowledge. Focused individual committed to building trusting relationships with key physicians and nurses by training, educating and selling them on our cutting-edge technologies. Must uphold all of the quality policies outlined within sales structure consistently and completely.

About the role: The MDM Developer is a critical role in the design and implementation of Master Data Management (MDM) Solutions at BSCI. He/she is responsible for following development standards and best practices, and will assist with requirements gathering/analysis, development, testing, documentation, and deployment tasks with some business-facing. This role will work independently and collaboratively with internal, external, offshore, onshore and nearshore teams. Your responsibilities will include: Develop and support MDM solutions Contribute to a team responsible for designing, developing, optimizing, and maintaining the master data (MDM) processes Understand overall data strategies and roadmaps Assemble large, complex sets of data to meet non-functional and functional requirements Partners with Solution Architects to perform source system analysis, identification of key data issues, data profiling and development of physical schemas for mastering data Follow best practices for data movement, data quality, and master data management Drives the technical design, development, optimization, error handling and support of data management initiatives Create and implement Master Data Management Solutions to ensure data standardization, quality, governance, enrichment and provide a single source-of-truth for the domains Participates in business meetings to understand data through stakeholder interviews and by defining, analyzing, and validating data Perform feasibility analysis, scoping exercises, and works with the project manager to prioritize deliverables Provides mentoring and support for junior developers Collaboratively drafts detailed documentation per standards Working knowledge with informatica in cloud and cloud native MDM Required qualifications: Bachelors Degree in Information Systems, Computer Science, or related field 3 plus years of experience as an Informatica MDM Developer Experience in PL/SQL ((advance queries, tuning) with RDBMS platforms in Agile Experience in Data Integration, MDM, Data Analysis, Modeling and Quality Assurance Proficiency in complex SQL statements and interpret results for accuracy and performance 3 plus years of experience with Informatica ETL workloads Technical understanding of data models, data management, business processes and tools, specifically Data Governance, Master Data Management, Data Modeling, Metadata Management, and Data Quality Working knowledge in MDM life cycle with strong focus on data and with implementing multiple master data domains (Customer, Products, Supplier) using Informatica MDM in cloud and IICS

About the Role: The Customer Care department is crucial in managing and administering the order management of medical equipment and processing orders and inquiries. You will join a dynamic international team supporting local Growth and Emerging Markets and global distributors in fulfilling product orders. Your role will involve managing order handling and ensuring an exceptional customer experience. Key Responsibilities Performing order entry or order management functions with high quality and delivering expected performance with the needed productivity. Utilizing your expertise in the German language to support the team by interpreting customer comments on faxes and aligning them with process knowledge to solve queries. Meeting all required metrics such as average handling time, quality targets, etc., as assigned per the process guidelines. Aligning with all queries shared by the local customer care team and providing resolutions based on information given by customers. Being efficient with MS Excel, PowerPoint, MS Word, and MS Outlook Teams. Creating required reports and presentations. Applying basic conceptual knowledge of theories, practices, and procedures within the job function. Performing assignments using existing procedures. Receiving guidance and direction from more senior-level roles/managers within the job function. Applying general business knowledge obtained through education or past experience with guidance from others. No supervisory responsibility; accountable for own contributions and meeting objectives with guidance from more senior-level roles/managers. Working within standardized procedures and practices to achieve objectives and meet deadlines. Exchanging straightforward information, asking questions, and checking for understanding. Compiling and organizing data/information to support discussions and inform decision-making. Requirements Minimum education level: University (Bachelor s Degree) Minimum 4-5 years of experience in Customer Service and working with order-to-cash processes, ideally in the Medical Devices/Medical Technology sector (or similarly regulated industry, e.g., Pharmaceuticals, etc.) Experience with and proficiency using SAP and the Microsoft Office suite of products (Excel, PowerPoint, Outlook) Excellent interpersonal and communication skills with a customer-centric mindset Highly organized Ability to manage a complex workload in a matrixed environment Willingness to learn, grow, and develop Business fluency in English - written and verbal is non-negotiable Proficiency in German language

Required Qualifications: Technical Expertise : Proven experience in administering IBM Integration Bus (IIB), IBM App Connect, and IBM MQ. Strong proficiency in Unix/Linux environments, including hands-on experience with Unix scripting. Familiarity with integration patterns, message flows, and data transformation processes. Experience : 10+ years of experience in EAI platform engineering, system administration, or a similar role in integration technologies. Analytical Skills : Strong problem-solving skills with the ability to diagnose and resolve complex technical issues efficiently. Collaboration : Excellent teamwork and communication skills, with a collaborative approach to working with cross-functional teams.

Responsible for providing mechanical engineering support in the maintenance of project DHF deliverables in Requirements Management (RM) tool for new and sustaining medical device products (invasive and non-invasive). Key Responsibilities: Read and interpret technical drawings, procedures, and protocols. Import and maintains the project documentation in online RM tool throughout all phases of NPD and Sustaining. Investigates and evaluates the compliance requirements driven from organization s QMS/Work Instructions and validate the same in templates developed in RM tool. Investigates and evaluates existing RM tools/technologies - JAMA, Polarion etc. Investigates compliance gaps in project documents and resolve them with project stake holders. Collaborate with cross-functional process, method, and teams to understand and implement solutions to resolve compliance gap issues in documents. Performs validation of patches and versions of RM tool as and when available. Support multiple projects across different time zones - Asia, Ireland, and North America Qualifications: Mechanical Engineering ( B.E./B.Tech) with 8-10 years of experience. Preferred experience in management of DHF documentation during full life cycle of medical device as per ISO 13485, and ISO 14971 Preferred experience in RM tools like JAMA, Polarion, DOORS, Cockpit. Knowledge of MS Office Tools - Word, Excel, PowerPoint. Strong attention to detail with good communication skills. Strong strategic / analytical thinking and problem-solving abilities, with a data-driven approach to decision-making. Ability to collaborate and work as a team player. Nice to have experience in product lifecycle management software and tools. Willingness to work in an agile environment.