Regulatory Affairs Jobs in Kashmik Formulation - Sanand, Gujarat

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Regulatory Affairs Jobs in Kashmik Formulation - Sanand, Gujarat

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Kashmik Formulation

time outline iconSanand, Gujarat, India

Posted on 05-01-2026

1 Vacancy

Description

  1. Job Title: Regulatory Affairs
  2. Location: Kashmik Formulation - Sanand, Gujarat
  3. Qualification: Bpharm
  4. Experience: 0 to 5 Years
  5. Prepare and submit regulatory dossiers for product registrations and approvals.
  6. Handle documentation and submissions to regulatory authorities (CDSCO, DCGI, etc.).
  7. Ensure compliance with national and international regulatory guidelines.
  8. Coordinate with QA, QC, R&D, and production teams for regulatory requirements.
  9. 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

BPharm (Bachelor Of Pharmacy)

Key Skills

Regulatory ComplianceDocumentationCoordination SkillsAttention to Detail

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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