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Philips is hiring experienced Post Market Surveillance (PMS) Specialists in Bangalore and Pune. If you have strong expertise in post-market surveillance, risk management, medical device regulations, ISO standards, and FDA/EU-MDR compliance, this opportunity is ideal for you. The role is crucial for ensuring product safety, quality, and regulatory alignment across global markets.
This article covers job responsibilities, eligibility, benefits, application details, and includes FAQs to help candidates apply confidently.
⭐ Job Responsibilities
As a Post Market Surveillance Specialist, your key responsibilities will include:
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Post Market Surveillance (PMS) Activities
- Create and maintain PMS Plans, PMS Reports, and PSURs
- Conduct Periodic Quality Review Board (PQRB) meetings
- Perform proactive & reactive surveillance—complaints, literature, regulatory databases
- Support complaint trending, investigation, signal assessment, and escalation
- Benchmark best practices and work closely with internal teams
Risk Management
- Facilitate post-market risk assessments, including:
- Health Hazard Evaluations (HHE)
- Issue impact assessments
- Support creation/review of Risk Management Plans, RM reports, FMEAs, and risk matrices
Regulatory Reporting & Safety
- Evaluate safety signals and recommend corrective actions
- Support FDA/EU-MDR reporting requirements
- Assist in decision-making for correction & removal
- Liaise with Medical Affairs, R&D, Complaint Handling, and Clinical Affairs
PMS & RM Support in Product Development
- Represent PMS function in multidisciplinary development teams
- Ensure PMS deliverables are integrated into product life cycle
- Provide inputs on product quality and risk-based insights
🎓 Eligibility & Qualifications
Required Education
- Bachelor’s degree in Medical Sciences, Healthcare Management, Industrial Engineering, Supply Chain Management, or equivalent.
Required Experience
- 4–8 years of experience in Post Market Surveillance within FDA/EU-MDR regulated medical device environments
- Strong knowledge of:
- 21 CFR 803, 806, 820
- ISO 13485, ISO 14971
- EU MDR, MDD (93/42/EEC)
- Canadian MDR (SOR/98-282)
- Proven experience in PMS Plans, PMS Reports, PSURs, and risk assessments
Preferred Skills
- Post-Market Surveillance mechanisms
- Quality Management Systems (QMS)
- Regulatory Documentation
- Complaint Handling
- Data Management
- Business Acumen
- Project Management
🌟 Why Join Philips?
- Hybrid working model (2 days WFO)
- Inclusive, diverse, and employee-friendly culture
- Opportunity to work on innovative healthcare technologies
- Career growth through multidisciplinary collaboration
- Impact millions by improving global patient safety
📌 Job Locations
- Bangalore
- Pune
📅 Important Dates
- Posted: Today
- Application Deadline: December 15, 2025
💼 How to Apply
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