Roles and ResponsibilitiesPrepare tender documents, including bid solicitation, bidding process, and contract award.Coordinate with internal teams (Technical, Commercial, Legal) to prepare tender submissions.Manage timely submission of tenders on GeM portal.Ensure compliance with government procurement procedures and regulations.Monitor and track progress of ongoing tenders from submission to closure.Desired Candidate Profile4-9 years of experience in Government E-Tendering or related field.Strong knowledge of e-procurement processes on GeM portal.Excellent communication skills for effective coordination with internal stakeholders.Ability to work independently with minimal supervision while meeting deadlines.Interested candidate mail their CVs at m.sneha@transasia.co.in

Role & Responsibilities Responsible for driving verification and validation activities for medical device NPIs including planning, resource management, execution. 1. Extensive knowledge of Verification and Validation of medical devices to enable defining V&V strategy for the products and executing them to fulfil the regulatory and quality requirements of the product.2. Develop verification plan for the NPI programs including, resource, budget, timelines. Execute as per plan and provide periodic status reports.3. Hire and manage the V&V team for product programs - assign daily task schedules and monitoring while managing any unforeseen delays. Manage traceability, Issue resolutions working closely with cross functional engineering and program team members Review specifications and technical design documents to provide timely and meaningful feedback for Engineering Verification & Validation activities.Own & Maintain the Verification, Validation & Process Validation infrastructure (SOP, Forms, SW tools, Jigs, Simulators, and Phantoms).Create detailed, comprehensive and well-structured V&V Plan, test protocols and reports, with traceability with Risk Analysis Matrix & Design Control documentation.Create Verification and Validation Procedures, execute tests, and document Results.Develop, implement and document verification techniques, test setups, equipment and environment required for System test executionExecution of Verification and Validation plans, including coordinating efforts of test personnel inside and outside the Design Verification and Validation group. Define & Execute the Usability & Ergonomic Verification Test protocols.Develop and execute reliability and integration tests for prototypes and products.Develop manufacturing process validation activities for NPI projects (IQ\OQ\PQ, Validation Plans, Sample size, Testing forms and Documentation).Maintain relevant chapters of DHF & DMR.Develop and implement of methodologies for collecting and analysing failure data and determining root cause of failures (FTA, investigation, SPR, etc.,).Coordinating failure analysis with other disciplines as necessary to lead to determination of root cause and close design defects.Ensure testing abides to Engineering Quality Procedures (QMS Quality Management System), Phased Review Discipline and regulatory needs of the applicable marketsParticipation in project meetings, project reviews, and specification reviews.Identify and report any quality or compliance concerns and take immediate corrective action as requiredPreferred candidate profile a. Bachelors or Masters Degree in Engineering with minimum 8 years of Verification and validation experience working with cross-functional teams in an industry environment b. Minimum 3 years of experience in leading verification and validation of NPI in medical devices industry.c. Proven Verification & Validation experience in medical device industry with a strong emphasis on problem solving, along with written and verbal skills Technical Qualifications:Experience in Verification and Validation, including test methodologies development at system-level for medical products that include Hardware and Software.Strong knowledge of testing methodologies and processes, including manual, automated, standards and compliance testingKnowledge and experience with Medical Device Quality Systems, ISO 13485, FDA.Knowledge and experience with environment, safety, bio-compatibility, sterility and essential performance tests (IEC 60601, EN 61508, ISO 10993-5, ISO 11135, etc.).Demonstrated skills for planning and coordinating verification and validation activities for NPI from design to Manufacturing transfer.Hands on experience in Root cause analysis methodologies, Demonstrated problem-solving and leadership skills.Strong technical orientation for understanding multi-disciplined systems.Good documentation skills and ability to communicate effectively at all levels of the organization.Can conform to shifting priorities, demands and timelines through analytical and problem-solving capabilities. Ability to effectively prioritize and execute tasks in a high-pressure environment.Multi-tasker, independent, punctual and accurate with excellent organizational skills, Team oriented, collaborative, good personal relationships.Familiarity with requirement, defect and software management toolsExperience designing, building, and maintaining instrumented test systems or electronic systemsAbility to work in a high paced, dynamic environment with a variety of people

1.Customer feedback calling 2. Pending call follow up and closure 3. SR creation and SR allocation 4. PM Due n Done Compliance 5. Pending Installation follow-up 6. Responding to Whatsapp ( Call Registration )7. Responding to SMS ( Call Registration) 8. Inbound call handling (customer complaints, queries) 9. PM calls correction and update 10. Installation calls allocation 11. Zoho CRM call logging, reports and MIS Interested candidates please mail their CVs at m.sneha@transasia.co.in

Design, develop and implement application software solutions on Linux using Python, C, C++ for innovative medical devices. 1. Design and implement the Software architecture as per the requirement specifications.2. Breaking down problems, Documenting problem statements and effort estimation.3. Adhering to Engineering methodologies.4. Design, develop and implement Application Software for a Computer Vision Driven Robotic Device while interfacing with embedded software.5.Troubleshoot any problems, defects and issues in the application software during development. MAJOR RESPONSIBILITIES:Design and Development of Software as per requirements.Writing clean, high-quality, high-performance, maintainable code while incorporating good design practices.Develop and support software including applications, hardware and sensor data integration, interfaces, and new functionality enhancements.Coordinate cross-functionally to ensure project meets business objectives and compliance standards.Support test and deployment of new products and features.Design and implement algorithms and software solutions, as per the specifications.Participate in code reviews. COMPETENCIES: Skills: C++ / C (must), Linux (highly desirable), LVGL (desirable), Experience/Exposure to Yocto & Poky (nice to have), multi-threaded applications / IPC Design & Development (Desirable),PythonDesirable: Experience in Linux, Embedded Systems Interfacing; with a solid Math background.Desirable: Exposure and Experience in Object Oriented DesignKnowledge and practice of applying Design Patterns - nice to have.Experience with Computer Vision, Image Processing Algorithms and Stereo Vision; and exposure to Kinematics & Robotics are desirable - nice to have. Knowledge & experience of working on Windows & Linux platform Experience with Agile or Scrum software development methodologies.Ability to plan, organize, and prioritize work. REQUIREMENT PROFILE: Bachelor's degree in computer science / information science / electrical / Electronics / Medical electronics engineering. 6+ years of industry experience.

Role & responsibilities 1. To ensure Preventive Maintenance of Instruments.2. To attend breakdown calls.3. To achieve AMC/CMC targets.4. To maintain records of spares in respective territories. - However record should be maintained in the system - not with individual.5. Timely despatch of spares to HO.6. To refurbish instruments in the territory assigned. 7. To ensure timely follow up for Payment.8. To support customer for application support. 9. To install instruments & impart training to customers. 10. To promote contracts, QC and consumables and achieve individual target.

PURPOSE OF THE POSITION:Design, develop and implement hardware architecture innovative medical devices and solutions. KEY RESULT AREAS:1. Define and develop the Hardware architecture for new generation of medical devices.2. Breaking down problems, Documenting problem statements and effort estimation.3. Implementing Engineering methodologies / practices in the team and drive adherence.Manage the hardware function to deliver innovative product solutions. RESPONSIBILITIES:1. Manage concept to production engineering - including high level design, detailed design, schematic entry, simulation, layout design, prototype assembly and logistics, board bring up, debugging, system integration, design verification and manufacturing handoff.2. Design electronic boards and interconnects comprising digital, Analog, power, microcontroller / microprocessor, precision low level Analog designs, A/D and D/a converts, monitor circuits and programable logic-based designs.3. Work closely with suppliers, sourcing, manufacturing and service teams to realize project goals.4. Ensure Design for manufacturing (DFM), Design for test (DFT), Design for reliability (DFR), compliance to regulatory requirements (IEC60601 and others as required).5. Work closely with project management to ensure alignment of plans with deliverables.6. Ensure conceptual completeness of the hardware engineering solution.7. Lead research and evaluation of technologies, Industry and Market trends to assist in product development8. Provide technology leadership, guidance and mentorship throughout your domain.9. Operate within an economic framework when analysing the impact of design decisions. REQUIREMENT PROFILE: (Qualification, No of yrs exp)a. Bachelors / Masters degree in Electrical / Electronics / Medical electronics engineering.b. 10+ years of industry experience in concept to delivery with around 4 years of medical devices design and development experience. c. Knowledge of regulations relating to hardware design in medical device industry. COMPETENCIES: (knowledge, skills and attitudes required to perform job):a. Experienced in end to end electrical and electronic hardware development cycle in digital, analog, power and microcontroller / microprocessor-based designs.b. Experience in interfacing real time sensors like force, position, distance, light, etc.,c. Thorough understanding of new product introduction process, regulatory compliance process and design history file documentation.d. Self-motivated to carry hands on work with the ability to debug and fix issues in hardware system.e. Demonstrated experience in design reviews through the product development lifecycle.f. Define requirements for firmware development, test automation tools development.g. Hands-on experience with schematic, layout Altium or Orcad and circuit simulation tools.h. Hands-on experience with signal and power integrity design.i. Ability to drive board bring up, performance testing and reliability demonstration.j. Positive attitude to explore, drive and passionate in excelling on the technology goals.k. Good communication skills to communicate with customers, research partners, business leaders and team members.Desired:l. Hands on experience with medical devices using motion control and / or robotics modules.m. n. Interfacing vision systems.

Role & responsibilities :Extraction of nucleic acid from virus, bacteria and human samples. Designing of primers and probes for conventional PCR, qPCR and LAMP.Standardization, optimization & production of molecular assays (PCR/qPCR/LAMP/Crispr).Calibration, verification and validation of developed assay.Development of controls, standards and secondary reference material. Troubleshooting and application support to the customers for developed assay.Development of protocol, procedure, SOP, IFU, work instructions related to the developed product.Preparation of documents for regulatory approvals of developed assay.To ensure smooth tech transfers and to establish good manufacturing practices and quality checks.Preferred candidate profile Expertise in RTPCR assay development

Role & responsibilities 1. New Product Development - FIA and Rapid.2. Documentation for WHO, CDSCO etc3. Train Team Members4. Support in Technology Transfer activitiesPreferred candidate profile Candidate should have handson experience in development of FIA and Rapid products.