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Manager - Regulatory Affairs Jobs in Cadila Pharmaceuticals Ltd - Ahmedabad, Gujarat

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Manager - Regulatory Affairs Jobs in Cadila Pharmaceuticals Ltd - Ahmedabad, Gujarat

work outline icon10 - 15 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Cadila Pharmaceuticals Ltd

time outline iconAhmedabad, Gujarat, India

Posted on 28-01-2026

1 Vacancy

Description

  1. Job Title: Manager - Regulatory Affairs
  2. Qualification: MPharm/BPharm
  3. Location: Cadila Pharmaceuticals Ltd - Ahmedabad, Gujarat
  4. Work Experience: 10 to 15 Years

Job Description

  1. Perform formulation development for new products.
  2. Conduct pre-formulation and compatibility studies.
  3. Develop robust, stable and cost-effective formulations.
  4. Execute lab-scale, pilot-scale & scale-up batches.
  5. Prepare development protocols, reports & SOPs.
  6. Support technology transfer to manufacturing.
  7. Coordinate with ADL for method development & validation.
  8. Monitor stability studies and recommend improvements.
  9. Assist in regulatory submissions (CTD/ANDA support).
  10. Ensure compliance with cGMP & data integrity.
  11. Provide technical support during process validation.

Take this opportunity to join Cadila Pharmaceuticals Ltd - Ahmedabad, Gujarat as a Manager - Regulatory Affairs in Ahmedabad, 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

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

DocumentationAnalytical SkillsDevelopmentCommunication Skills

About Organization

Cadila Pharmaceuticals Ltd, Ahmedabad, Gujarat, is a leading pharmaceutical company committed to innovation, regulatory compliance, and high-quality healthcare solutions. The company is expanding its regulatory affairs team and inviting applications for this role. The responsibilities include managing regulatory submissions and approvals, ensuring compliance with local and global regulatory requirements, preparing regulatory reports and dossiers, coordinating with cross-functional teams, tracking regulatory changes, and maintaining regulatory documentation. This opportunity offers strong exposure to regulatory affairs processes, professional development, and long-term career growth in a structured and supportive pharmaceutical environment.

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