Sanofi Hyd Hiring Freshers – R&D (Regulatory Affairs)
- R&D Ancillary Document Coordinator Vacancy at Sanofi – Hyderabad
- Career Opportunity for Life Science & Regulatory Affairs Graduates
- About Sanofi
- Job Overview: R&D Ancillary Document Coordinator
- Key Responsibilities:
- Qualifications & Skills Required
- Educational Background:
- Required Experience:
- Why Join Sanofi?
- How to Apply
- Job Snapshot Table
R&D Ancillary Document Coordinator Jobs in Hyderabad | BSc/MSc Life Sciences, Regulatory Affairs
Apply for R&D Ancillary Document Coordinator role at Sanofi, Hyderabad. BSc/MSc Life Sciences or Regulatory Affairs required. Fresher & experienced roles open.
R&D Ancillary Document Coordinator Vacancy at Sanofi – Hyderabad
Career Opportunity for Life Science & Regulatory Affairs Graduates
Sanofi is inviting applications for the position of R&D Ancillary Document Coordinator in Hyderabad, India. This is a promising opportunity for graduates with a background in Life Sciences, Pharmaceutical Sciences, Regulatory Affairs, or related fields. The company offers a permanent role with international exposure, advanced tools, and dynamic work culture for individuals eager to pursue a career in regulatory operations and documentation coordination.
About Sanofi
Sanofi is a leading global healthcare organization driven by the pursuit of scientific innovation to improve people’s lives. With operations spanning across continents, Sanofi offers countless opportunities for professional growth, especially through its advanced global hubs. The Hyderabad hub is a key part of its global operations, streamlining processes and accelerating scientific breakthroughs.
Job Overview: R&D Ancillary Document Coordinator
Key Responsibilities:
- Coordinate and manage ancillary document requests for global regulatory portfolios.
- Provide country-specific guidance on regulatory submissions.
- Advise internal teams on document regulations and timelines.
- Create and maintain ancillary document templates (e.g., CPP forms).
- Coordinate with vendors to execute requests and ensure timely shipping.
- Maintain documentation and metadata in Vault RIM.
- Ensure compliance with Health Authority standards and internal SOPs.
- Partner with Digital teams to evaluate and implement new technologies.
Qualifications & Skills Required
Educational Background:
- Bachelor’s or Master’s degree in:
- Life Sciences
- Regulatory Affairs
- Pharmaceutical Sciences
- Biotechnology
- Chemistry
- Biology
- Medical Sciences
Required Experience:
- 0–3 years (freshers and experienced professionals welcome).
- Experience in Regulatory Operations or Regulatory Affairs preferred.
- Proficiency in document management systems like Vault RIM.
- Strong command of English (written & verbal).
- High attention to detail and process orientation.
- Strong project coordination and communication skills.
Why Join Sanofi?
- Work on impactful projects contributing to global health.
- International mobility and career growth opportunities.
- Industry-leading health and wellness benefits.
- Inclusive and diverse workplace culture.
- At least 14 weeks of gender-neutral parental leave.
How to Apply
👉 Apply here: https://jobs.sanofi.com/en/job/-/-/2649/24702177472
Application Closing Date: June 30, 2025
Job Snapshot Table
| Company Name | Current Vacancies in Departments | Required Education | Experience Required |
|---|---|---|---|
| Sanofi | R&D (Regulatory Affairs) | BSc/MSc Life Sciences, Regulatory Affairs | 0–3 years |
To apply for this job please visit jobs.sanofi.com.