Software Engineer JOB SUMMARY Under general direction, participates as high-level technical expert in design development, coding, testing, and debugging new software or significant enhancements to existing software for third party customers, project leads, and management. Works with technical staff to understand problems with software and develops specifications to resolve them. Develops and/or provides technical leadership in the development of software involving application of new technologies with significant technical risk. ESSENTIAL DUTIES Act as high-level technical expert, addressing problems of systems integration, compatibility, and multiple platforms. Lead a large development team in the design of highly complex software systems for internal and external customers and is responsible for project completion as required. Designs, develops, operates and maintains software and firmware components and computing systems software to apply to, and integrate with engineering, scientific and manufacturing requirements. Independently design and develop new software products or major enhancements to existing software for internal and external customers. Provides functional and empirical analysis related to the design, development, and implementation of software operating systems, including, but not limited to, utility software, development software, and diagnostic software. Perform feasibility analysis on potential future projects to management. Performs and Approves code and test reviews. Exercise considerable latitude in determining technical objectives of assignment. Advances new techniques or advances the state-of-the-art. Demonstrates expert computer science fundamentals such as design patterns, data structures, OOP and software design. Mentors less-experienced software development staff. Defines software development best practices. OTHER DUTIES AND RESPONSIBILITIES : Represent the organization as the prime technical contact on contracts and projects. Interact with senior external personnel on significant technical matters often requiring coordination between organizations. May act as team leader on complex projects. May participate in the development of test strategies, devices, and systems. Holds self and team accountable for adherence to Agile principles and practices. MINIMUM QUALIFICATION REQUIREMENTS : Education Bachelor's degree in computer science or, equivalent of education and experience sufficient to successfully perform the essential functions of the job may be considered. Experience : Minimum 4 years experience Must have experience with mission critical applications, preferably medical products or devices. Knowledge of regulatory requirements preferred. Skills Possess proficiency in object engineering and applications development using Embedded C++. Experience with modern C++ highly preferred (C++11/14/17) Must have knowledge of unit and component level testing preferably within the Catch framework using BDD style. Skilled in Developing technical solutions to complex problems which require the regular use of ingenuity and creativity. Ability to use object-oriented systems composed of objects that communicate with one another using explicitly designed interfaces, an (OO) methodologies. Experience with embedded operating systems and tools to build those such as Yocto and/or Buildroot. Conducts research in design, development, testing and utilization of electronic data processing hardware and software and/or electrical components, circuitry, processes, packaging and cabinetry for CPU's and peripheral equipment. Inter Process Communication (IPC) concepts Experience in cross compiler, Firmware development, board bring up activities. Good to have experience in RTOS, VxWorks, shell script, JSON, GIT HUB, Angular JS, Jira. Work beyond routine nature of tasks, utilizing specialized knowledge and technologies. Individual must be team-oriented with excellent attitude and vision. Knowledge and use of relevant PC software applications and skills to use them effectively. Demonstrated ability to communicate effectively both verbally and in writing. -Or- An equivalent competency level acquired through a variation of these qualifications may be considered.

Jon Description -Mechanical Design EngineerProven experience in the design & development and analysis of mechanical systems, structures and enclosures preferably related to medical equipment High level of expertise in SolidWorks (part, assembly, sheet metal, drawing, simulations, Tol Analyst) and AutoCAD Strong understanding of mechanical engineering principles, selection of standard components, material properties and manufacturing processes Experience in pressure die casting and plastic injection molding process is a plus • Proficiency in engineering calculations and FEA simulation Proficiency in GD&T and tolerance stack up analysis Proficiency in design and manufacturing of parts with tight tolerance specifications Proficiency in technical documentation and creating detailed manufacturing drawings Knowledge of industry standards and regulations relevant to mechanical design, preferably medical equipment design Experience in prototyping, testing and validation of mechanical systems and components Familiarity with Design for manufacturing (DFM) and Design for Assembly (DFA) principles Knowledge of PLM tool like PTC Windchill is a plus Excellent problem solving and analytical skills with ability to identify and resolve complex mechanical issues Strong communication and interpersonal skills Self-motivated and able to work independently with a strong sense of ownership and accountability Ability to collaborate with global cross functional teams Knowledge of standards related to medical equipment design preferred.OTHER DUTIES AND RESPONSIBILITIES Colloborate with global cross functional teams Experience 3~5 years of experience in the design and development of mechanical systems preferably in medical product development or manufacturing .

Architect, implement, and maintain a robust configuration management strategy.ESSENTIAL DUTIES : Demonstrate a solid understanding of configuration management principles, fundamentals, architectures, protocols, standards, tools, and methodologies. • Support well-organized large-scale development, maintenance, and release effort across all medical device functional areas. Take ownership of planning, implementing, and monitoring the configuration management system for the R&D organization. Enforce regulatory criteria, standards, product development principles, and engineering best practices. Support configuration items and their attributes, relationships, dependencies, versions, revisions, and releases including software branch support for multiple fielded software versions. Anticipate future configuration management challenges and develop a strategy to effectively prevent or minimize negative outcomes. Allow development to proceed simultaneously along more than one path while maintaining the relationships between the different paths. Establish and enforce baseline integrity. Maintain all current and future variants of a product lifecycle. Simultaneously manages several in-parallel, in-flight projects across several domains. • The configuration management strategy must support engineering analysis of proposed design changes to determine the effect on the overall system. The configuration management strategy must assist engineers in identifying and implementing measures to mitigate risks associated with configuration changes.SKILLS: Extensive knowledge of the product development lifecycle, from planning and development through to release and maintenance. Meticulous attention to detail in all tasks and projects. • Skilled in fostering open communication and collaboration, encouraging input from others and contributing to a positive team environment. Effective presentation skills, capable of delivering technical information to both technical and non-technical audiences and adept at responding to inquiries from various stakeholders. Superior written and verbal communication abilities, ensuring clear and effective communication of complex information across diverse audiences. Problem-solving and analytical skills. Apply critical thinking skills to analyze problems and develop innovative solutions. Proficient in identifying and resolving issues promptly. Make timely decisions involving appropriate stakeholders, ensuring efficient problem resolution and project execution. Proven ability to communicate effectively both verbally and in writing, fostering strong relationships and clear understanding. Demonstrated leadership skills, including strong interpersonal skills and the capacity to lead through influence rather than authority. Strong listening and observational skills, able to quickly grasp audience needs and adjust communication style accordingly. Excellent organizational and time management skills and proper prioritization, ensuring efficient workflow and deadlines consistently met. Proactively pinpoint and take ownership of issues, including thorough follow-through to resolution. • Able to work independently with minimal oversight, demonstrating initiative and selfmotivation. • Knowledge and effective use of relevant PC software applications and skills to use them effectively. Strong work ethic characterized by dedication and reliability in team-based settings

JOB TITLE: Senior Electronics Engineer and Electronics EngineerJOB SUMMARYWe are looking for a highly skilled and experienced Senior Embedded Systems Engineer to join our dynamicteam. In this role, he/ she will:• Be responsible for Designing, developing, and maintaining embedded systems and software formedical devices.• Work closely with cross-functional teams to ensure the successful integration of hardware andsoftware components.• Be responsible for optimizing system performance, ensuring reliability, and meeting projectdeadlines.• Have a strong background in embedded systems, excellent problem-solving skills, and the ability towork independently as well as part of a team.• Be expected to stay up to date with the latest industry trends and technologies and apply thisknowledge to improve our products and processes.• Independently conduct design change impact assessment, coordinate technical reviews of the changes, conduct failure analysis and potential risk impact assessment as part of a cross-functional Team.ESSENTIAL DUTIES• Translate user and business requirements into detailed product requirement specifications anddesign specifications.• Apply design controls with extensive knowledge of ISO 13485, ISO 14971, IEC 62304, IEC 62366, andIEC 60601 for medical device development.• Design and develop embedded systems and software for medical devices.• Collaborate with cross-functional teams to integrate hardware and software components.• Optimize system performance and ensure reliability.• Troubleshoot and resolve issues related to embedded systems.• Document design specifications, test procedures, and results.• Stay current with industry trends and technologies.• Participate in code reviews and provide constructive feedback.• Mentor junior engineers and provide technical guidance.• Contribute to the continuous improvement of development processes.• Ensure compliance with industry standards and regulations.• Manage project timelines and deliverables.• Apply Six Sigma and Lean principles to enhance efficiency and minimize waste.• Define integration and verification plans with experience in budgeting adequate resources and time for execution of the plans• Create, maintain and release Design History File (DHF), Device History Record (DHR), Device MasterRecord (DMR)• Conduct Technical reviews to root cause issues, perform tradeoff analysis, document key designconsiderations for future reference OTHER DUTIES AND RESPONSIBILITIES• Work direction responsibility may include technicians and junior engineers.• May work with manufacturing and other functional groups on manufacturing and regulatory compliance issues.• May contribute to the establishment of business objectives, goals, budgets, and costs.MINIMUM QUALIFICATION REQUIREMENTS Education• Bachelors degree or equivalent of education and experience sufficient to successfully perform theessential functions of the job may be considered.• Bachelor of Science degree or Master of Science degree in Engineering preferred.Experience• Minimum of 5 years of experience is required for a Senior Electronics Engineer and minimum 3 yearsof experience for Electronics Engineer.• Preferable Minimum of 3 years of experience in the medical device field preferred for Senior Engineerand minimum 1 years of experience for Electronics Engineer.Skills1. Strong Knowledge of hardware design in Analog, high frequency Digital Circuit Design and RF circuits design2. Hardware design experience with I2C, SPI, CAN, UART, USB, Ethernet, BLE protocols on Micro- Controllers (preferably ARM)3. Must have completed a number of Embedded Systems based projects based on 8/16/32 bit microcontrollers preferably for medical equipments4. Experience with resource limited Embedded RTOS or Embedded Linux in SBC5. Proficient with PCB design tools or EDA Software (Altium or OrCAD)6. Proficient in hardware debugging of high frequency circuits digital circuits7. Develops hardware architecture and component selection based on equipment requirement8. Hardware Design consideration for EMI/EMC and ESD and safety standards for medical equipments and test requirements9. Strong knowledge for detailed design documentation of the hardware circuits on component level10. Experience in DFMEA and Risk analysis and product development life cycle

SYSTEM ENGINEERING JOB SUMMARY- Senior systems engineer translates the user needs and business needs into the specifications that drive design, implementation, testing of products that are used for collection of blood and blood components. Senior systems engineer will practice design controls in compliance with the quality management systems to deliver on products that are effective, safe and compliant. In this role you are expected to coordinate the design activities in collaboration with various stakeholders including mechanical, electrical, software, quality, manufacturing and commercial Teams. As a senior systems engineer you are expected to independently conduct design change impact assessment, coordinate technical reviews of the changes, conduct failure analysis and potential risk impact assessment as part of a cross-functional Team ESSENTIAL DUTIES • Translate user and business requirements into detailed product requirement specifications and design specifications. Apply design controls with extensive knowledge of ISO 13485, ISO 14971, IEC 62304, IEC 62366, and IEC 60601 for medical device development. Lead multidisciplinary design efforts to ensure seamless integration and timely delivery. • Collaborate globally to integrate mechanical, electrical, and software components, achieving functional and reliability goals. • Lead design changes to implement and enhance features for blood collection platforms, ensuring quality and regulatory compliance. • Independently conduct technical reviews with stakeholders to meet project design objectives. • Perform failure analyses to prioritize testing and ensure design completeness and product quality Communicate and collaborate effectively to align teams and streamline workflows. • Support design transfer to enable successful commercialization of complex products. • Use systems thinking to design complex platforms integrating equipment, software, and disposables. • Apply knowledge of manufacturing processes tailored to diverse product types like electronics, mechanical design and plastics. Define and manage project scope to optimize resources and avoid scope creep. Lead defect management meetings to achieve actionable outcomes and maintain good documentation practices. • Develop and approve test protocols to ensure functional testing and maximize reuse for multiple configurations. Apply Six Sigma and Lean principles to enhance efficiency and minimize waste. • Define integration and verification plans with experience in budgeting adequate resources and time for execution of the plans Create, maintain and release Design History File (DHF), Device History Record (DHR), Device Master Record (DMR) Conduct Technical reviews to root cause issues, perform tradeoff analysis, document key design considerations for future reference. Skills • Proficient in configuration management for complex medical device platforms including hardware, software and disposables • Knowledgeable in evaluating designs for serviceability and manufacturability • Practice the creation, maintenance of Design History files for medical device products • Awareness of EUMDR, FDA QSR for technical documentation, labeling and clinical evaluation • Develop and oversee test methods to demonstrate the design has implemented the necessary functionality • Conduct design analysis necessary to evaluate the completeness of specifications, testing • Utilize failure analysis to determine if the designs are effective in meeting the user and business needs • Evaluate the designs for serviceability and manufacturability • Mentor junior engineers on the practice of systems thinking • Manage projects independently to lead changes to existing features and incorporate new features for the product platforms used in collecting blood and blood components • Experience in conducting risk analysis for defects to demonstrate the safety and efficacy of medical device platforms • Proficient in using requirements management tools like Doors, Windchill RV&S • Proficient in using test management tools like ALM for test case management • Experience in using SysML for describing the complex design using tools like CATIA Magic Cyber Systems Engineer, PTC Modeler or Enterprise Architect.

Possess proficiency in object engineering and applications development using Embedded C++. Experience with modern C++ highly preferred (C++11/14/17) • Must have knowledge of unit and component level testing preferably within the Catch framework using BDD style. • Skilled in Developing technical solutions to complex problems which require the regular use of ingenuity and creativity. • Ability to use object-oriented systems composed of objects that communicate with one another using explicitly designed interfaces, an (OO) methodologies. • Experience with embedded operating systems and tools to build those such as Yocto and/or Buildroot. • Conducts research in design, development, testing and utilization of electronic data processing hardware and software and/or electrical components, circuitry, processes, packaging and cabinetry for CPU's and peripheral equipment. • Inter Process Communication (IPC) concepts • Experience in cross compiler, Firmware development, board bring up activities. • Good to have experience in RTOS, VxWorks, shell script, JSON, GIT HUB, Angular JS, Jira. • Work beyond routine nature of tasks, utilizing specialized knowledge and technologies. • Individual must be team-oriented with excellent attitude and vision. • Knowledge and use of relevant PC software applications and skills to use them effectively. • Demonstrated ability to communicate effectively both verbally and in writing.

JOB TITLE: Senior Electronics Engineer and Electronics EngineerJOB SUMMARYWe are looking for a highly skilled and experienced Senior Embedded Systems Engineer to join our dynamicteam. In this role, he/ she will:• Be responsible for Designing, developing, and maintaining embedded systems and software formedical devices.• Work closely with cross-functional teams to ensure the successful integration of hardware andsoftware components.• Be responsible for optimizing system performance, ensuring reliability, and meeting projectdeadlines.• Have a strong background in embedded systems, excellent problem-solving skills, and the ability towork independently as well as part of a team.• Be expected to stay up to date with the latest industry trends and technologies and apply thisknowledge to improve our products and processes.• Independently conduct design change impact assessment, coordinate technical reviews of the changes, conduct failure analysis and potential risk impact assessment as part of a cross-functional Team.ESSENTIAL DUTIES• Translate user and business requirements into detailed product requirement specifications anddesign specifications.• Apply design controls with extensive knowledge of ISO 13485, ISO 14971, IEC 62304, IEC 62366, andIEC 60601 for medical device development.• Design and develop embedded systems and software for medical devices.• Collaborate with cross-functional teams to integrate hardware and software components.• Optimize system performance and ensure reliability.• Troubleshoot and resolve issues related to embedded systems.• Document design specifications, test procedures, and results.• Stay current with industry trends and technologies.• Participate in code reviews and provide constructive feedback.• Mentor junior engineers and provide technical guidance.• Contribute to the continuous improvement of development processes.• Ensure compliance with industry standards and regulations.• Manage project timelines and deliverables.• Apply Six Sigma and Lean principles to enhance efficiency and minimize waste.• Define integration and verification plans with experience in budgeting adequate resources and time for execution of the plans• Create, maintain and release Design History File (DHF), Device History Record (DHR), Device MasterRecord (DMR)• Conduct Technical reviews to root cause issues, perform tradeoff analysis, document key designconsiderations for future reference OTHER DUTIES AND RESPONSIBILITIES• Work direction responsibility may include technicians and junior engineers.• May work with manufacturing and other functional groups on manufacturing and regulatory compliance issues.• May contribute to the establishment of business objectives, goals, budgets, and costs.MINIMUM QUALIFICATION REQUIREMENTS Education• Bachelors degree or equivalent of education and experience sufficient to successfully perform theessential functions of the job may be considered.• Bachelor of Science degree or Master of Science degree in Engineering preferred.Experience• Minimum of 5 years of experience is required for a Senior Electronics Engineer and minimum 3 yearsof experience for Electronics Engineer.• Preferable Minimum of 3 years of experience in the medical device field preferred for Senior Engineerand minimum 1 years of experience for Electronics Engineer.Skills1. Strong Knowledge of hardware design in Analog, high frequency Digital Circuit Design and RF circuits design2. Hardware design experience with I2C, SPI, CAN, UART, USB, Ethernet, BLE protocols on Micro- Controllers (preferably ARM)3. Must have completed a number of Embedded Systems based projects based on 8/16/32 bit microcontrollers preferably for medical equipments4. Experience with resource limited Embedded RTOS or Embedded Linux in SBC5. Proficient with PCB design tools or EDA Software (Altium or OrCAD)6. Proficient in hardware debugging of high frequency circuits digital circuits7. Develops hardware architecture and component selection based on equipment requirement8. Hardware Design consideration for EMI/EMC and ESD and safety standards for medical equipments and test requirements9. Strong knowledge for detailed design documentation of the hardware circuits on component level10. Experience in DFMEA and Risk analysis and product development life cycle