As a Senior Design Engineer at BD in Bengaluru, India, you will lead design verification activities, develop test methods, and ensure compliance with medical device quality systems. This full-time, on-site role involves collaborating with cross-functional teams to drive transformative MedTech solutions.
Requirements
Strong experience in Medical Device Verification & Validation (V&V).
Knowledge of Design Controls, Risk Management, and regulatory requirements.
Hands-on experience with statistical analysis, DOE, and MSA/Gage R&R.
Proficiency in verification protocol development and defect investigation.
Experience with CAD models and engineering drawings is preferred.
Skills & Responsibilities
Medical Device V&V: Lead design verification strategies, protocols, test plans, and reports to ensure healthcare equipment safety and reliability.
Statistical Analysis: Analyze verification data using DOE and MSA/Gage R&R methods to provide data-driven recommendations.
Defect Investigation: Investigate defects and failures using structured root cause analysis techniques to assess product performance.
Cross-functional Collaboration: Partner with Systems Engineering, R&D, Quality, and Regulatory teams while maintaining Design History File documentation.
Potential transition routes: People from Quality Assurance or Systems Engineering roles may bring relevant regulatory and testing skills, alongside meeting strong verification and design control requirements.
Job description
We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
Key Responsibilities
Lead design verification activities, including development of verification strategies, protocols, test plans, and reports.
Develop, complete, and optimize product performance, reliability, and safety testing specific to healthcare equipment.
Analyze verification data using appropriate statistical methods and provide data-driven recommendations.
Develop test methods, measurement systems, and validation approaches to support verification activities.
Investigate defects, failures, and design variances using structured root cause analysis techniques.
Interpret verification results and assess product performance, robustness, and manufacturing stability.
Support requirements development, traceability, and verification coverage assessments.
Collaborate with Systems Engineering, R&D, Quality, Regulatory, Manufacturing, Marketing and Operations teams.
Maintain Design History File (DHF) documentation and ensure compliance with Design Controls and Quality Management System requirements.
Lead technical reviews, present findings to collaborators, and mentor junior engineers.
Required Skills & Qualifications
Strong experience in Medical Device Verification & Validation (V&V).
Knowledge of Design Controls, Risk Management, and regulatory requirements for medical devices.
Hands-on experience with statistical analysis, DOE, MSA/Gage R&R, and data interpretation.
Proficiency in verification protocol/report development and defect investigation.
Experience translating product requirements into verifiable test methods and acceptance criteria.
Familiarity with DFSS, reliability engineering, and DFX principles.
Working knowledge of Power BI or equivalent data visualization tools.
Experience with CAD models, engineering drawings, and verification documentation is preferred.
Excellent technical communication, presentation, and multi-functional collaboration skills.
Preferred Qualifications
Experience supporting products in US and European regulatory markets.
Knowledge of ISO 14971, ISO 13485 Design Control requirements, and medical device quality systems.
Experience leading verification workstreams in new product development or sustaining engineering projects.
Why Join Us?
To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.
