Medical Writing Specialist

Zimmer Biomet · Bengaluru | Hybrid

🏭Company: Zimmer Biomet

📍Location: Bengaluru, Karnataka, India

💻Work Mode: Hybrid (3 Days in Office)

📅Experience: 2+ Years preferred | Min. Bachelor’s in Life Sciences/Engineering

📌Job #: 10355 · Corporate Careers

🕐Employment: Full-Time

About Zimmer Biomet

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. Zimmer Biomet offers robust ERGs, a flexible working environment, competitive total rewards, wellness incentives, and a culture of recognition — committed to 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, National Joint Registry (NJR) data analysis, ensures traceability and compliance, and collaborates cross-functionally to deliver audit-ready documentation.

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; 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.
Supports methodological consistency across product lines.
Participates in internal peer reviews.
Manages timelines for assigned deliverables and performs quality control checks for formatting, references, and traceability.
Escalates and resolves compliance or risk concerns as needed.

What Makes You Stand Out

Strong scientific and technical writing skills.
Basic working knowledge of medical device clinical and regulatory documentation.
Ability to execute literature strategies and appraise evidence.
Ability to analyze National Joint Registry (NJR) data.
Understanding of global medical device regulations and post-market obligations.
Strong analytical and data synthesis skills with effective cross-functional communication.
Ability to manage multiple documents and deadlines with high attention to detail.
Organizational skills and awareness of audit/inspection readiness and compliance expectations.

Your Background & Requirements

Education

Bachelor’s in Health/Life Sciences or Engineering preferred. Associate’s Degree + 4 yrs or High School + 6 yrs also considered.

Experience

2+ years in medical or regulatory writing preferred. Medical device industry experience required. CEP/CER/PMS/PMCF/SSCP experience required.

Authoring experience in Systematic Literature Searches and CER updates for medical devices under MDR.
CEPs, CERs, PMS, PMCF, and SSCP documents — some experience required.
Bachelor’s Degree in Health, Life Sciences or related field + 2 years relevant experience; or Associate’s Degree + 4 years; or High School Diploma + 6 years.
Preferred: Degree in Health, Life Sciences or related field; 2+ years in medical or regulatory writing.
Experience in the medical device industry is required.
Very good English oral and written; critical thinking and attention to detail.
Travel: Up to 5%.

Apply on Zimmer Biomet Careers Portal

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