Medical Writing Specialist

Role Overview Zimmer Biomet is a globally recognised medical technology company with close to a century of innovation in improving patient mobility. As a Medical Writing Specialist based out of Bengaluru, you will independently author regulatory clinical documents and contribute to audit-ready submissions that directly support patient safety and product compliance. This is a hybrid role requiring three days in office per week, offering a collaborative and growth-oriented work environment. Key Responsibilities - Independently author 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 - Execute National Joint Registry (NJR) data analysis and systematic literature search strategies, and document appraisal outcomes - Draft clinical safety and performance summaries along with benefit-risk analyses - Ensure full traceability across data sources and applicable regulatory requirements - Maintain template compliance and keep all documentation audit-ready at all times - Coordinate with Regulatory, Clinical, and Product Development teams to finalise document drafts - Perform quality control checks covering formatting, references, and traceability - Manage timelines for assigned deliverables and support methodological consistency across product lines - Participate in internal peer reviews and escalate compliance or risk concerns when required Required Qualifications - Bachelor's degree in Health, Life Sciences, Engineering, or a related field with a minimum of 2 years of relevant experience, or equivalent combination of education and experience - Prior experience in medical or regulatory writing, preferably within the medical device industry - Working knowledge of regulatory clinical documents including CEPs, CERs, PMS, PMCF, and SSCP - Understanding of global medical device regulations and post-market surveillance obligations - Strong scientific and technical writing skills with excellent command of written and spoken English - Strong analytical, data synthesis, and cross-functional communication skills - High attention to detail, organisational ability, and willingness to learn evolving regulatory requirements - Readiness to travel up to 5 percent as needed Why Join Us At Zimmer Biomet, every team member contributes to a mission that enhances the lives of patients around the world, with a Zimmer Biomet product or technology improving a patient's mobility every 8 seconds. You will benefit from robust employee resource groups, flexible working arrangements, competitive total rewards, wellness incentives, and a culture that values recognition, inclusion, and continuous development.

- Bachelor's degree in Health, Life Sciences, Engineering, or related field - Minimum 2 years of experience in medical or regulatory writing - Experience in the medical device industry is required - Knowledge of Clinical Evaluation Plans, CERs, PMS, PMCF, and SSCP documentation - Ability to execute systematic literature searches and appraise clinical evidence - Familiarity with National Joint Registry (NJR) data analysis - Understanding of global medical device regulations including MDR - Excellent written and verbal communication skills in English - Strong analytical thinking and attention to detail - Ability to manage multiple documents and meet deadlines - Awareness of audit and inspection readiness requirements

- Hybrid work model with flexibility - Robust employee resource groups (ERGs) - Wellness incentives and health programmes - Location-specific competitive total rewards - Culture of recognition and performance awards - Learning and development opportunities