🧬 Regulatory Affairs Job Opening at Sanofi – Apply Before June 30!
Are you a life science graduate with a passion for compliance, precision, and global pharmaceutical documentation? Sanofi, a global healthcare leader, is currently hiring for the role of R&D Ancillary Document Coordinator in Hyderabad, and this might just be your next big career move!
With a legacy of innovation and patient care, Sanofi is one of the world’s most respected pharmaceutical brands. Their Hyderabad location offers not only top-notch professional experience but also the opportunity to work in a supportive and progressive workplace culture.
🌍 About the Company – Why Sanofi?
Sanofi is known for developing therapies that transform lives. Their mission is to chase the miracles of science and improve healthcare across continents. Sanofi offers a work culture that promotes inclusivity, work-life balance, and continuous learning. They also support international career mobility, ensuring your growth isn’t limited by geography.
Whether you’re dreaming of shaping global dossiers or improving submission processes, this job offers real-world exposure to regulatory functions that matter.
📄 Job Role: R&D Ancillary Document Coordinator
Sanofi is looking for skilled professionals who can manage and coordinate regulatory documentation for global submissions. This isn’t just a back-office role—it’s an essential part of ensuring that life-saving drugs make it to the market quickly and compliantly.
📍 Location: Hyderabad
💼 Experience Required: Minimum 2 Years
🎓 Qualification:
- B.Pharm or M.Pharm
- Bachelor’s degree in Regulatory Affairs, Life Sciences, or related field
🔍 Key Responsibilities
As an R&D Ancillary Document Coordinator, you will have 4 major areas of responsibility. Let’s break them down:
✔️ 1. Ancillary Document Management
- Collect, track, and manage supporting documents essential for regulatory submissions
- Ensure full compliance with international and local pharmaceutical regulations
- Collaborate with third-party vendors and cross-functional teams for document flow
- Maintain accurate tracking tools and submission timelines
✔️ 2. Regulatory Support
- Advise teams on regional and global documentation requirements
- Draft and review Certificates of Pharmaceutical Product (CPP) and other forms
- Upload and manage all regulatory documents in Vault RIM, tagging with correct metadata
- Stay updated with changing regulatory expectations in various markets
✔️ 3. Process Enhancement
- Suggest improvements to the digital documentation systems
- Collaborate with the Global Regulatory Affairs (GRA) and IT teams
- Work towards reducing turnaround time for document requests and approvals
✔️ 4. Cross-Department Coordination
- Act as a liaison between internal stakeholders and external vendors
- Ensure high-quality dossier submissions in a timely manner
- Report delays, risks, and errors to the regulatory management team
👩🔬 Ideal Candidate Profile
To be successful in this role, Sanofi is looking for someone who is:
✅ Academically Qualified:
- Holds a Bachelor’s or Master’s in Pharmacy, Regulatory Affairs, Life Sciences, or similar discipline
✅ Professionally Experienced:
- Has 2+ years in pharmaceutical regulatory affairs or documentation roles
- Experience with Vault RIM, MS Office, and Adobe Acrobat is a must
- Familiar with global submission formats and regulatory expectations
✅ Skill-Oriented:
- Excellent project management and organizational skills
- Strong attention to detail and ability to meet strict timelines
- Fluent in English (written and spoken)
- A good team player with strong interpersonal communication
🌟 Why Join Sanofi?
Still wondering if this is the right place for you? Here’s why this opportunity stands out:
🌐 Global Growth:
Sanofi offers international mobility and exposure to global markets.
👩⚕️ Healthcare & Wellness:
Access to health insurance, parental leave, and wellness initiatives.
🧠 Innovation Culture:
You’ll work on cutting-edge processes that directly impact patient access to medicine.
🫱🏻🫲🏽 Inclusive Workplace:
Sanofi believes in diversity, equity, and inclusivity—offering equal opportunities to all.
🕐 Important Dates
📅 Application Deadline: June 30, 2025
📍 Location: Hyderabad (On-site role)
“Regulatory work isn’t just paperwork—it’s the backbone of safe, legal, and effective access to medicine across the globe.”
💡 Final Thoughts
This role is perfect for professionals who are passionate about organization, precision, and public health. If you’ve ever wanted to play a part in bringing innovative healthcare products to market while managing vital global submissions, this is your calling.
Don’t miss this golden opportunity to grow your career with a brand that’s shaping the future of medicine.
🖼 Suggested Canva Image Placements
📌 Header Image Caption:
“Join Sanofi’s Global Regulatory Team – Where Compliance Meets Innovation”
📌 Mid-Post Image Caption:
“Document Coordination in Action: Collaborating for Global Pharmaceutical Submissions”
Let me know if you’d like to generate the Canva image text overlays or create another job-based blog post in the same style!Tools
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