Medical Writing Specialist

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

Independently authors standard sections of regulatory clinical documents with limited supervision. Executes literature strategies, execute National Joint Registry (NJR) data analysis, ensures traceability and compliance, and collaborates crossfunctionally to deliver audit-ready documentation.

Work Location: Bangalore Work Mode: Hybrid (3 Days in office)

How You'll Create Impact

• Independently authors standard sections of Clinical Evaluation Plans (CEPs), Clinical Evaluation Reports (CERs), Post-

Market Surveillance (PMS), Post-Market Clinical Follow-up (PMCF), and Summary of Safety and Clinical Performance (SSCP) documents

• Executes NJR analysis and literature search strategies and documents appraisal outcomes

• Drafts clinical safety and performance summaries and benefit–risk analyses

• Ensures traceability across data sources and regulatory requirements

• Maintains template compliance and audit-ready documentation

• Coordinates with Regulatory, Clinical, and Development partners to finalize drafts