Healthcare & Pharmaceuticals
Regulatory Affairs Manager
Lead regulatory submissions for regulated and semi-regulated markets at a formulations business.
- Location
- Ahmedabad, Gujarat
- Experience
- 7–12 years
- Compensation
- ₹20-32 LPA
- Reference
- NM-RA-1064
Sample listing. This is demonstration data, not a live vacancy, which is why no JobPosting structured data is emitted for it.
Full-timeOn-siteQuality & Regulatory
About the opportunity
Part of a regulatory team of eight supporting a growing export portfolio.
Responsibilities
- Prepare and manage dossier submissions for target markets
- Own regulatory queries and deficiency responses through to approval
- Maintain lifecycle management for approved products
- Partner with R&D, quality and manufacturing on regulatory requirements
Requirements
- M.Pharm or equivalent with seven or more years in regulatory affairs
- Experience preparing submissions for regulated markets
- Working knowledge of eCTD and relevant regulatory guidelines
- Strong technical writing capability
Skills
- Regulatory Submissions
- eCTD
- Lifecycle Management
- Technical Writing
- Posted
- 6 Aug 2026
- Applications close
- 6 Nov 2026
- Reference ID
- NM-RA-1064
For candidates
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