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Hiring Regulatory Associates
Remote / Gurugram / Mumbai
0.5–2 Years
Regulatory Affairs
CMC Module 3
🏢 About Company
Syneos Health is a global CRO providing clinical development and commercialization services. The company contributes to a majority of global drug approvals and offers strong career growth in regulatory affairs.
💼 Job Roles
- Regulatory Associate (EU CMC Module 3) – Remote / Gurugram
- Regulatory Affairs Associate – Mumbai
📌 Key Responsibilities
- Prepare CMC Module 3 documents
- Support IND, NDA, MAA submissions
- Manage lifecycle activities (variations, renewals)
- Perform QC & regulatory research
- Handle drug registrations & documentation
- Coordinate with global teams
🎓 Eligibility
- B.Pharm / M.Pharm / Life Sciences
- 0.5–2 years experience (internship accepted)
- Knowledge of CMC & regulatory processes
💻 Skills Required
- Regulatory writing & documentation
- Microsoft Office
- Analytical & communication skills
- Attention to detail
📚 Helpful Resources
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Make sure your qualifications and experience align with the role requirements.
Kindly read the entire job description carefully before applying. Make sure your qualifications and experience align with the role requirements.
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