Life Sciences Job Opening in Medical Writing at Sanofi
Sanofi is seeking a detail-oriented Medical Regulatory Writer with experience in writing scientific and safety documents to join its Global Hub team in Hyderabad. Suppose you’re passionate about regulatory science, pharmacovigilance, and medical documentation, and have 2+ years of experience in the healthcare or pharmaceutical industry. In that case, this is your opportunity to work in a dynamic, global healthcare organization focused on improving lives through cutting-edge innovation and compliance excellence.
- Job Title: Medical Regulatory Writer
- Location: Hyderabad, Telangana, India
- Job Requisition ID: R2815700
- Application Deadline: August 14, 2025
About the Company:
The Sanofi Global Hub is an internal Sanofi resource organization based in India, established to centralize processes and activities supporting Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, as well as Data & Digital functions. Sanofi Global Hub aims to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations within Sanofi, globally.
About the Job:
Sanofi Global Hub is seeking a Medical Regulatory Writer to join our team in Hyderabad. The ideal candidate will be responsible for writing and editing high-quality safety documents and medical sections of various reports, ensuring compliance with internal and external standards.
Key Responsibilities for Medical Regulatory Writer Opportunity at Sanofi
- Author and edit high-quality regulatory documents, including safety summaries, periodic benefit-risk evaluation reports (PBRER), product alerts, trial transparency documents, and more.
- Collaborate closely with cross-functional teams, including scientific communications, pharmacovigilance, regulatory affairs, clinical teams, and corporate affairs.
- Plan and present data for regulatory use in compliance with internal and external guidelines.
- Track document posting, ensure audit-readiness, and maintain up-to-date knowledge of regulatory policies.
- Collaborate with external vendors and internal teams to develop and execute regulatory writing plans, enhancing content delivery processes.
- Assist with Q&A documentation and standby statements related to product alerts.
- Support stakeholders by analyzing medical regulatory writing needs and producing relevant deliverables for global teams.
Qualifications for Medical Regulatory Writer Opportunity at Sanofi
- Education: Advanced degree in life sciences, pharmacy, or medicine (e.g., PhD, Master’s, MBBS, BDS, BAMS, BHMS, PharmD).
- Experience: Minimum 2 years of regulatory medical writing experience in the pharmaceutical or healthcare industry.
- Skills:
- Strong command over regulatory guidelines (ICH, GCP/GVP).
- Excellent writing and scientific editing skills.
- Ability to interpret and summarize complex scientific data.
- Proficiency in stakeholder and vendor management.
- Familiarity with systems for tracking and archiving regulatory documentation.
- Language: Fluent in English (reading, writing, speaking).
Keywords: Medical Regulatory Writer, Sanofi Hyderabad, regulatory medical writing jobs, PBRER writing jobs, clinical documentation, ICH GCP medical writer, healthcare regulatory careers India. Life Sciences Job Opening in Medical Writing at Sanofi
