Medical Writing Sr 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 leads complex, high-risk clinical deliverables. Defines evidence strategies, develops robust benefit risk positions, and provides expert review and mentorship to ensure high-quality, compliant documentation.

Work Location: Bangalore

Work Mode: Hybrid (3 Days in Office)

How You'll Create Impact

Leads authorship of complex, high-risk post-market clinical deliverables such as Clinical Evaluation Reports (CERs) & Summary of Safety and Clinical Performance (SSCP)

Defines and executes National Joint Registry (NJR) analysis as well as literature search strategies, appraisal criteria, and evidence synthesis approaches

Interprets clinical and safety data to develop robust benefit–risk arguments

Provides expert peer review of medical writing deliverables

Mentors junior writers

Partners with Clinical, Regulatory, and Development teams on evidence strategy

Addresses autonomously Notified Body and regulatory questions related to clinical documentation

Leads complex review cycles and issue resolution

Contributes to improvements in templates, methodologies, and writing standards

Functions as subject matter expert for medical writing aspects during Audit

What Makes You Stand Out

Advanced scientific writing expertise

Deep knowledge and independent ownership of Clinical Evaluation Plans (CEPs), CERs, Post-Market Surveillance (PMS), Post-Market Clinical Follow-up (PMCF), SSCP, and regulatory expectations

Strong evidence evaluation and benefit–risk analysis capability

Ability to mentor and provide expert-level review

Strong stakeholder influence skills

Problem-solving in regulatory and NB interactions

Ability to manage complex, high-risk deliverables

Commitment to high quality and continuous improvement

Ability to efficiently prioritize multiple project tasks simultaneously, focusing on critical aspects while maintaining

strategic oversight to deliver high-quality results and meet deadlines

Ability to escalate and resolve compliance or risk concerns

Your Background

Bachelor's Degree in Health, Life Sciences or related field and 4 years of relevant experience, or Associate's Degree & 6 years of relevant experience, or High School Diploma or Equivalent and 8 years of relevant experience

Preferred: Degree in Health, Life Sciences or related field

4+ years medical or regulatory writing experience

Physical Requirements

Travel Expectations

Up to 5%

EOE/M/F/Vet/Disability