Health Science Job at Zimmer Biomet in Bangalore | Apply Now
An exciting health science job opportunity is available at Zimmer Biomet for a Post Market Surveillance Specialist in Bangalore, Karnataka. This role offers professionals the chance to work with a global medical technology leader while contributing to regulatory compliance, post-market clinical follow-up, and patient safety. Candidates exploring Zimmer Biomet jobs and specialized jobs in Bangalore within the medical device sector will find this position highly relevant.
Job Details
- Position: Post Market Surveillance Specialist
- Location: Bangalore, Karnataka, India
- Job Category: Corporate Careers
- Job ID: 8669
- Employment Type: Full-Time
About the Company
Zimmer Biomet is a global medical technology leader with nearly 100 years of experience in advancing patient mobility. A Zimmer Biomet product or technology enhances a patient’s mobility every 8 seconds worldwide. The organization operates with a strong focus on innovation, inclusion, employee development, wellness initiatives, and performance recognition, offering competitive rewards and a flexible working environment across locations.
Job Description
This health science job is responsible for post-market surveillance (PMS) assignments, including document ownership of initial PMS plans, revised plans, tracking of Post Market Clinical Follow-up (PMCF) commitments, and scheduling of PMS review according to the PMS schedule.
Education and Experience
- Experience Required: 2+ years
- Education: Bachelor’s degree in health science or a similar discipline
Qualifications
Required Skills
- Thorough knowledge of global medical device regulations related to post-market surveillance, including Medical Device Directive and revisions, ISO 14155, FDA Sections 515 and 522, and FDA MDR requirements, is preferred.
- Seniority is determined by level of autonomy, critical thinking ability, project ownership, and capacity to work independently.
- Excellent English verbal and written communication skills.
Desired Skills
- Direct experience with PSURs and PMS plans is preferred; candidates from related areas such as product surveillance or complaints handling may also be considered.
- Prior experience with clinical trials is considered an asset.
- For junior roles, motivated candidates with quality or product surveillance backgrounds and proactive PMS exposure are considered.
- Strong project management and organizational skills with the ability to manage multiple projects simultaneously while meeting deadlines.
Key Responsibilities
- Acts as document owner for Post Market Surveillance activities, including Initial PMS Plans (PMSP) and PMS Review (PMSR) records, working with Regulatory Affairs to ensure documentation is reviewed and aligned with Notified Bodies when applicable.
- Ensures Post Market Clinical Follow-up (PMCF) commitments are clearly documented within relevant PMSPs, communicated to the clinical research department, and aligned with Notified Bodies.
- Schedules and coordinates PMS team reviews for proactive and vigilance activities according to established schedules, gathering inputs from cross-functional stakeholders and escalating at-risk findings to senior management.
- Tracks execution of PMS plans according to requirements and reports to management on on-track, delayed, and at-risk PMS commitments.
- Manages PMS action items to ensure deadlines are met and conducts routine audits of PMCF commitments against PMSPs to maintain quality and transparency.
