Technical Product Owner
On-siteBengaluru, Karnataka, India
Job Summary
Own and author software requirements derived from system and product needs, ensuring clarity, unambiguity, and testability. Maintain requirements documentation throughout the product lifecycle and collaborate with architects to derive Detailed Software Requirements Specifications (DSWRS). Manage the product backlog, decompose items into features, epics, and user stories, and ensure end-to-end traceability between requirements and verification artifacts. Partner with global cross-functional teams to drive verification, validation, and change management while bridging product needs with engineering execution. This IC role focuses on requirements engineering and backlog ownership for ENT, Plastic & Refractive medical device portfolios. The candidate must possess 10+ years of experience in regulated medical device environments with hands-on proficiency in tools like DOORS or Polarion.
Required Qualifications
- 10+ years of experience in Own and author software development within the medical device industry, working in regulated environments
- Proven hands-on experience with requirements engineering, including ownership of software requirements documentation (SRS, SWRS, or equivalent)
- Strong working knowledge of regulated software development lifecycles, including experience with structured development processes and design controls
- Hands-on experience using requirements management tools such as DOORS, Polarion, Codebeamer, or equivalent tools in regulated environments
- Experience working with cross-functional global teams, including Product Management, Engineering, and Quality/Regulatory functions
- Strong communication and stakeholder management skills
Desired Qualifications
- Experience in domains such as surgical visualization, medical imaging, or surgical devices
- Familiarity with Agile/Scrum methodologies within regulated environments
- Understanding of risk management and quality processes in medical devices
- Experience deriving or supporting test specifications from software requirements
- Exposure to cybersecurity considerations in medical device software
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