Sanofi, a global biopharmaceutical leader, has announced two exciting R&D documentation roles at its Hyderabad Hub: R&D Electronic Document Specialist and R&D Senior Electronic Document Specialist. These roles are critical to ensuring high-quality regulatory submissions, including eCTD, IND, NDA, and BLA documentation, supporting Sanofi’s mission to bring life-changing medicines to patients worldwide.
Professionals with experience in regulatory document management, electronic submissions, Vault RIM, and EDMS systems will find this an excellent opportunity to build a long-term career in pharmaceutical R&D operations.
📌 Open Positions at Sanofi Hyderabad
1️⃣ R&D Electronic Document Specialist
📍 Location: Hyderabad
🕒 Job Type: Full-time
🆔 Requisition ID: R2836340
📅 Last Date to Apply: January 16, 2026
2️⃣ R&D Senior Electronic Document Specialist
📍 Location: Hyderabad
🕒 Job Type: Full-time
🆔 Requisition ID: R2836339
📅 Last Date to Apply: January 16, 2026
📝 Key Responsibilities (Both Roles)
- Prepare, format, and validate regulatory documents and dossiers for submission readiness (eCTD, CTD, IND, NDA, BLA)
- Ensure electronic submission compliance, including file formats, metadata, XML tagging, and naming conventions
- Perform quality control checks (linking errors, formatting issues, inconsistencies)
- Manage version control, embargoed documents, and document integrity
- Collaborate with Regulatory Affairs, Clinical, Nonclinical, CMC, QA, ITS, and R&D teams
- Support document publishing and compilation
- Maintain accurate documentation and audit trails within EDMS
- (Senior role) Provide training, process improvement initiatives, and regulatory intelligence support
🎓 Eligibility & Qualifications
✅ Education
- Bachelor’s degree in Regulatory Affairs, Life Sciences, Pharmacy, IT, or related discipline
- Relevant industry experience may be considered equivalent
✅ Experience & Skills
- Experience in electronic document preparation for regulatory submissions
- Strong knowledge of eCTD structure, CTD modules, and global regulatory requirements (FDA, EMA)
- Hands-on experience with Veeva Vault RIM, EDMS, Adobe Acrobat, MS Office
- Understanding of regulatory processes across drug development stages
- Excellent attention to detail and compliance mindset
- Strong English communication skills (written & spoken)
- Ability to adapt to new technologies including AI-enabled documentation tools
💼 Why Join Sanofi?
- Work in a future-focused global R&D hub
- Exposure to end-to-end regulatory submissions
- Career growth through international and cross-functional opportunities
- Competitive compensation and comprehensive benefits
- Inclusive and diverse work culture aligned with Sanofi’s ALL IN initiative
- Opportunity to help shape best practices in R&D documentation
💰 Salary (Estimated)
- R&D Electronic Document Specialist: ₹10 – ₹16 LPA
- R&D Senior Electronic Document Specialist: ₹16 – ₹24 LPA
(Salary may vary based on experience and internal evaluation)
📥 How to Apply?
Application Link For R&D Electronic Document Specialist
Application Link For R&D Senior Electronic Document Specialist
