Cadila Pharmaceuticals Limited is inviting applications for the position of Executive – Regulatory Affairs (API) at its Dholka, Gujarat facility. This is an excellent opportunity for M.Sc graduates with 1 year of experience who are looking to build a strong career in API regulatory affairs, dossier preparation, and regulatory compliance within a reputed pharmaceutical organization.

If you are searching for Regulatory Affairs API jobs in Gujarat, pharma regulatory executive vacancies, or Cadila Pharma jobs, this opening could be the right next step in your career.

📌 Job Overview

• Company: Cadila Pharmaceuticals Limited
• Department: R&D – Regulatory Affairs (API)
• Position: Executive – Regulatory Affairs (API)
• Location: Dholka, Gujarat
• Qualification: M.Sc
• Experience: Minimum 1 Year

🔬 Key Responsibilities

• Preparation and compilation of API regulatory dossiers (CTD/eCTD).
• Handling DMF submissions, responses, and lifecycle management.
• Coordination with R&D, QA, and other departments for regulatory documentation.
• Review and update of regulatory documents as per global guidelines.
• Support regulatory compliance activities for API products.

🎓 Qualifications & Skills

• M.Sc in relevant discipline.
• 1 year experience in Regulatory Affairs (API).
• Knowledge of ICH, USFDA, EMA, and other regulatory guidelines.
• Good documentation, communication, and coordination skills.

💼 Why Join Cadila Pharmaceuticals?

• Work with a well-established Indian pharmaceutical company.
• Exposure to global regulatory submissions.
• Career growth in the API regulatory domain.
• Professional work environment and learning opportunities.

📲 How to Apply

Application Link