Wanted Clinical Evaluation Medical Writer at Medtronic

At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives.

Post : Clinical Evaluation Medical Writer

Job Description
• Prepare, edit, and review clinical and regulatory documents, including Clinical Evaluation Reports, clinical study reports or summaries, Summary of Safety and Clinical Performance reports, Periodic Safety Update Reports, and responses to Notified Body questions.
o Develop clear, accurate, and timely responses to audit and submission-related queries.
o Maintain databases of relevant peer-reviewed literature and clinical evidence.
o Critically appraise, analyze, summarize, and discuss clinical evidence from all available sources.
o Conduct comprehensive literature searches and perform critical evaluations of clinical evidence.
o Develop state-of-the-art assessments for assigned product families in alignment with their intended purpose.
• Prepare and edit manuscripts, abstracts, clinical study documents, scientific reports, special data summaries, monographs, comprehensive reviews, scientific exhibits, and other medical communication materials for regulatory submissions or internal use, as required.
• Collaborate regularly with cross-functional teams to gather and analyze data related to the safety and performance of medical devices and provide solution-oriented recommendations.
• Monitor evolving safety regulations, guidance documents, and industry expectations to support ongoing compliance.
• Apply knowledge of ISO 13485, ISO 14971, EU MDR, and applicable product-specific industry standards.
• Independently identify, assess, and analyze relevant clinical data from scientific publications and other credible sources.

Candidate Profile
• B.Pharma + M.Pharma , M.Sc. / Master’s degree in Pure or Applied Sciences, including Biochemistry, Biotechnology, Microbiology, Nursing, and other relevant Life Sciences disciplines, MBBS degree or a Doctorate in Pure or Applied Sciences.
• 4-8 years experiences as a medical/clinical writer in medical device and or pharmaceutical industry. A mix is preferred in case of pharma
• Knowledge of US / EU Quality Systems regulations, ISO 13485, ISO 14971, 21 CFR part 820, 21 CFR part 11, EUMDR and product specific industry standards
• Strong written, organizational, and communication skills, with a flexible and team-oriented approach.
• Strong attention to detail, effective planning skills, and the ability to manage multiple priorities under time-sensitive conditions.
• Proficiency in English, including reading, writing, and verbal communication.
• Demonstrated learning agility and commitment to continuous professional development.
Nice to Have :
• Experience working effectively with global and cross-functional teams.
• Relevant medical writing industry certifications.

Additional Information
Experience : 4-8 years
Qualification : B.Pharma + M.Pharma , M.Sc.
Location : Nanakramguda, Hyderabad
Industry Type : Pharma/ Healthcare/ Clinical research
Job ID : R72925
End Date : 30th October 2026