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 adaptable 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 ExpectIndependently authors standard sections of regulatory clinical documents with limited supervision. Executes literaturestrategies, execute National Joint Registry (NJR) data analysis, ensures traceability and compliance, and collaborates crossfunctionallyto deliver audit-ready documentation.Work Location: BangaloreWork Mode: Hybrid (3 Days in office)How You'll Create ImpactIndependently 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) documentsExecutes NJR analysis and literature search strategies and documents appraisal outcomesDrafts clinical safety and performance summaries and benefit–risk analysesEnsures traceability across data sources and regulatory requirementsMaintains template compliance and audit-ready documentationCoordinates with Regulatory, Clinical,



and Development partners to finalize draftsSupports methodological consistency across product linesParticipates in internal peer reviewsManages timelines for assigned deliverablesFollows established proceduresPerforms quality control checks for formatting, references, and traceabilityAbility to escalate and resolve compliance or risk concernsWhat Makes You Stand OutStrong scientific and technical writing skillsBasic working knowledge of medical device clinical and regulatory documentationAbility to execute literature strategies and appraise evidenceAbility to analyze National Joint Registry (NJR) dataUnderstanding of global medical device regulations and post-market obligationsStrong analytical and data synthesis skillsEffective cross-functional communicationAbility to manage multiple documents and deadlinesHigh attention to detail and commitment to accuracy Willingness to learn regulatory requirementsOrganizational skills and ability to manage multiple deliverablesAwareness of audit/inspection readiness and compliance expectationsYour BackgroundResponsible for authoring Systematic Literature Searches and Clinical Evaluation Reports (CERs) updates for medical devices under Medical Device Regulation (MDR)Bachelor's Degree in Health, Life Sciences or related field and 2 years of relevant experience, or Associate's Degree and4 years of relevant experience, or High School Diploma or Equivalent and 6 years of relevant experiencePreferred: Degree in Health, Life Sciences or related fieldPreferred: 2+ years experience in medical or regulatory writingExperience in the medical device industry is required 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 – some experience required.Bachelor’s degree in life sciences, engineering or related fields is preferred.Very good English oral and written. Critical thinking and attention to detailTravel ExpectationsUp to 5%EOE/M/F/Vet/Disability

📌 Medical Writing Specialist (Bengaluru)
🏢 Zimmer
📍 Bengaluru