Senior Regulatory Affairs Specialist
Moribus Pharma is seeking a Senior Regulatory Affairs Specialist to manage regulatory documentation and submissions for their medical and cosmetic product lines in Surat. The role involves ensuring compliance with international standards and collaborating with cross-functional teams for product approvals. Candidates must have 3-5 years of experience in dossier preparation and submission. The position requires strong analytical skills and a background in pharmacy or life sciences.
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Experience
3-5 years
Function
Research
Work mode
Onsite, India
Company
Tier 2
What you will work on
Moribus Pharma is seeking a Senior Regulatory Affairs Specialist to manage regulatory documentation and submissions for their medical and cosmetic product lines in Surat. The role involves ensuring compliance with international standards and collaborating with cross-functional teams for product approvals. Candidates must have 3-5 years of experience in dossier preparation and submission. The position requires strong analytical skills and a background in pharmacy or life sciences.
TAL's take
Role at a mid-tier pharma company with a well-defined, niche scope, but lacking specific growth or project impact details.
Very clear scope regarding regulatory documentation, dossiers, and compliance within the pharmaceuticals/cosmetics domain.
Must haves
- 3-5 years experience in Pharmaceutical Dossier preparation
- Proficiency in Regulatory Documentation preparation and review
- Understanding of Regulatory Compliance
- Experience in product classification and registrations
- Ability to manage Regulatory Submissions
- Bachelor's degree in pharmacy, life sciences, or related field
Tools and skills
About the company
unfamiliar company, default mid-tier