Randstad is hiring for a Regulatory Affairs Associate in Gurgaon, India, within the Global Regulatory Affairs department. The position requires candidates with 3–5 years of Regulatory Affairs experience in the pharmaceutical or medical-device industry, along with hands-on experience in dossier preparation, CDSCO submissions, Veeva Systems, and data management.
Job Details
| Details | Information |
|---|---|
| Position | Regulatory Affairs Associate |
| Department | Global Regulatory Affairs |
| Location | Gurgaon, India |
| Experience | 3–5 years |
| Industry | Pharmaceutical or Medical-Device |
Position
Regulatory Affairs Associate
The Regulatory Affairs Associate will work within the Global Regulatory Affairs department, with a focus on regulatory workflows, dossier preparation, CDSCO submissions, Veeva Systems, and data management.
Responsibilities
- Prepare regulatory dossiers.
- Support CDSCO submissions and Indian regulatory workflows.
- Work with Veeva Systems.
- Handle data management activities within the pharmaceutical or medical-device industry.
Eligibility & Qualifications
Candidates should have:
- 3–5 years of experience in Regulatory Affairs.
- Experience in the pharmaceutical or medical-device industry.
- Hands-on experience with dossier preparation.
- Experience with CDSCO/Indian regulatory workflows and submissions.
Required Skills
- Strong written communication skills.
- Strong verbal communication skills.
- Proven expertise in CDSCO/Indian regulatory workflows.
- Dossier preparation and submissions.
- Proficiency with Veeva Systems.
- Data management experience.
- Pharmaceutical or medical-device industry experience.
Application Details
Interested candidates who meet the requirements can share their CV at sahana.s@randstad.in.