Post Market Surveillance Specialist Jobs at Zimmer Biomet
- Zimmer Biomet Hiring Post Market Surveillance Specialist in Bangalore | Medical Device Regulatory Jobs
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Background:
- Experience Required:
- Skills Required:
- Location & Salary
- Application Process
- Why This Role Matters in Healthcare
- Frequently Asked Questions (FAQs)
- 1. Is this role suitable for freshers?
- 2. What is Post Market Surveillance?
- 3. What regulations should I know?
- 4. What career growth can I expect?
- Summary
Zimmer Biomet Hiring Post Market Surveillance Specialist in Bangalore | Medical Device Regulatory Jobs
A high-impact opportunity is now open for professionals in medical device safety and regulatory compliance. Zimmer Biomet is hiring a Post Market Surveillance (PMS) Specialist in Bangalore with a hybrid work model. This role is ideal for candidates with 2+ years of experience in pharmacovigilance, product surveillance, or clinical research within the medical device or healthcare industry.
This position plays a critical role in ensuring patient safety, regulatory compliance, and lifecycle monitoring of medical devices across global markets.
Company Overview
Zimmer Biomet is a global leader in medical technology with nearly 100 years of innovation in improving patient mobility and quality of life. The company’s products and technologies impact millions of patients worldwide, with a device used every few seconds globally.
Known for its strong regulatory framework and innovation-driven culture, Zimmer Biomet operates across multiple international markets and follows stringent compliance standards including FDA, ISO, and EU MDR guidelines.
Job Role & Responsibilities
As a Post Market Surveillance Specialist, you will manage PMS activities, documentation, and regulatory compliance for medical devices.
Key Responsibilities:
- Own and manage Post Market Surveillance Plans (PMSP) and Reports (PMSR)
- Track and manage Post Market Clinical Follow-up (PMCF) commitments
- Coordinate PMS reviews and cross-functional stakeholder inputs
- Monitor PMS activities and report risks, delays, and compliance status
- Support regulatory alignment with Notified Bodies and global authorities
- Conduct audits and ensure quality of PMS documentation
- Manage project timelines and ensure timely completion of PMS activities
Eligibility / Qualifications
Educational Background:
B.Pharmacy, M.Pharmacy, BSc, MSc (Life Sciences, Biomedical, Biotechnology), Engineering
Experience Required:
- Minimum 2+ years in pharmacovigilance, product surveillance, or clinical research
Skills Required:
- Strong understanding of medical device regulations (FDA, ISO 14155, EU MDR)
- Knowledge of PMS, PMCF, and safety reporting processes
- Strong project management and organizational skills
- Excellent communication and stakeholder management abilities
- Advanced proficiency in Microsoft Office and Excel
Location & Salary
- Location: Bangalore, Karnataka, India
- Work Mode: Hybrid (3 days office)
- Job Type: Full-time
- Salary: Competitive salary package with benefits
Application Process
Interested candidates can apply through the official careers page:
Apply Here: https://careers.zimmerbiomet.com/us/en/job/ZBUZBRUS8669EXTERNALENUS/Post-Market-Surveillance-Specialist?
Candidates are encouraged to apply early as positions may close quickly.
Why This Role Matters in Healthcare
Post Market Surveillance professionals ensure that medical devices remain safe and effective after they are launched in the market. Their work directly impacts patient safety and regulatory compliance.
This role is critical in maintaining global healthcare standards and ensuring continuous monitoring of product performance.
Frequently Asked Questions (FAQs)
1. Is this role suitable for freshers?
No, candidates must have at least 2 years of relevant experience.
2. What is Post Market Surveillance?
It involves monitoring the safety and performance of medical devices after they are released in the market.
3. What regulations should I know?
FDA regulations, ISO 14155, EU MDR, and global PMS guidelines.
4. What career growth can I expect?
You can grow into roles such as Regulatory Affairs Specialist, Safety Manager, or Clinical Compliance Lead.
Summary
| Category | Details |
|---|---|
| Company | Zimmer Biomet |
| Vacancies | Post Market Surveillance Specialist |
| Required Education | B.Pharmacy, M.Pharmacy, BSc, MSc, Engineering |
| Experience | 2+ Years |
To apply for this job please visit careers.zimmerbiomet.com.
