
Regulatory Affairs Jobs in Kashmik Formulation - Sanand, Gujarat
Kashmik Formulation
Sanand, Gujarat, India
Posted on 05-01-2026
1 Vacancy
Description
- Job Title: Regulatory Affairs
- Location: Kashmik Formulation - Sanand, Gujarat
- Qualification: Bpharm
- Experience: 0 to 5 Years
- Prepare and submit regulatory dossiers for product registrations and approvals.
- Handle documentation and submissions to regulatory authorities (CDSCO, DCGI, etc.).
- Ensure compliance with national and international regulatory guidelines.
- Coordinate with QA, QC, R&D, and production teams for regulatory requirements.
- Maintain and update regulatory files, databases, and product licenses.
Take this opportunity to join Kashmik Formulation - Sanand, Gujarat as a Regulatory Affairs in Sanand, Gujarat and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.
Category
Pharmaceuticals
Functional Area
Regulatory Affairs / Pharmacovigilance
Preferred Education
Key Skills
About Organization
Kashmik Formulation Pvt. Ltd. is a pharmaceutical manufacturing company headquartered in Ahmedabad, Gujarat, India. It was incorporated in January 2017 and has grown into a trusted name in pharma contract manufacturing, branded generics, and supply of high-quality healthcare products. Kashmik serves domestic and international markets, supplying medicines in India and exporting to overseas regions. The company operates with large daily manufacturing capacities (e.g., crores of tablets per day) and maintains WHO-GMP compliance to ensure quality and safety at industrial scale.
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