Medical Writing Specialist
Zimmer Biomet · Karnataka, India
Medical AffairsCompany career page
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Role summary
Medical writing specialist role focused on authoring regulatory clinical documentation for medical devices. The position involves independent writing of clinical evaluation reports, literature analysis, and cross-functional collaboration to ensure compliance and audit readiness.
What they're looking for
- Bachelor's degree in health or life sciences with 2 years relevant experience, or equivalent education/experience combination
- Medical device industry experience required
- Strong scientific and technical writing skills with proficiency in English
- Knowledge of medical device clinical and regulatory documentation standards
- Ability to execute literature searches and appraise clinical evidence
What you'll be doing
- Author clinical evaluation plans, reports, and post-market surveillance documentation independently
- Execute National Joint Registry data analysis and literature search strategies
- Draft clinical safety summaries, performance analyses, and benefit-risk assessments
- Coordinate with regulatory, clinical, and development teams to finalize documentation
- Perform quality control checks and ensure traceability and compliance
Privacy & handoff
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