APDM Pharmaceuticals Private Limited is expanding its regulatory team and inviting applications for the role of Executive / Sr. Executive – Regulatory Affairs at its Ahmedabad head office. This is an excellent opportunity for professionals seeking regulatory affairs jobs in Ahmedabad with exposure to global markets like the US and EMEA.
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If you have 4–6 years of experience in dossier preparation and regulatory compliance, this pharma regulatory affairs job offers strong career growth, structured work policies, and a collaborative environment.
Key Responsibilities
- Preparation and submission of regulatory dossiers for US and EMEA markets (mandatory)
- Handling regulatory queries and ensuring compliance with global standards
- Maintaining documentation and regulatory records
- Coordinating with cross-functional teams (R&D, QA, Production)
- Monitoring regulatory updates and industry intelligence
- Working knowledge of eCTD submissions and labeling (preferred)
Qualifications & Experience
- Education: B.Pharm or M.Pharm
- Experience: 4–6 years in regulatory affairs
- Strong understanding of global regulatory guidelines
- Experience in dossier compilation and submissions
Job Details
- Position: Executive / Sr. Executive – Regulatory Affairs
- Location: Ahmedabad, Gujarat, India
- Openings: 2
- Industry: Pharmaceutical / Regulatory Affairs
Benefits & Work Culture
- 1st & 3rd Saturdays off
- Attractive HR policies
- Opportunity to work on international regulatory submissions
- Growth-focused pharmaceutical work environment
How to Apply
Interested candidates can share their updated CV at:
📧 career@apdmpharma.com
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