Careers at Swift
Regulatory Affairs
For professionals who can support regulatory submissions, product documentation, and compliance requirements across pharmaceutical markets.
Responsibilities
- Prepare, review, and maintain regulatory dossiers and supporting documentation.
- Coordinate with quality, production, and formulation teams for submission-ready records.
- Track regulatory requirements, product approvals, and documentation updates.
Preferred Profile
- B.Pharm, M.Pharm, or a relevant life sciences background.
- Working knowledge of pharmaceutical regulations and dossier documentation.
- Strong written communication, accuracy, and attention to detail.
Work Location
Swift Life Sciences Pvt. Ltd.
D-1, Sara Industrial Estate Ltd., Rampur, Dehradun, Uttarakhand - 248197, India
Originally posted:
Last date to apply: (11:59 PM IST)