Ferring India Hiring Executive – Regulatory Affairs & Pharmacovigilance | Mumbai

Ferring India Hiring Executive – Regulatory Affairs & Pharmacovigilance | Mumbai | Medical Jobs India

Mohit March 17, 2026

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Executive – Regulatory Affairs & Pharmacovigilance

Ferring Pharmaceuticals

Mumbai

1+ Years

Regulatory Affairs

Pharmacovigilance

🏢 About Ferring

Ferring Pharmaceuticals is a globally recognized specialty biopharmaceutical company focused on reproductive medicine, gastroenterology, and urology. The company is known for its patient-centric innovation and strong global presence in healthcare and clinical development.

📌 Job Overview

Role: Executive – Regulatory Affairs & Pharmacovigilance
Company: Ferring Pharmaceuticals
Location: Mumbai, India
Experience: 1+ Year
Employment Type: Full-Time

🔬 Key Responsibilities

Safety reporting and pharmacovigilance activities
Follow-up for additional safety information
PSUR submission to Indian regulatory authorities
Preparation and submission of regulatory dossiers
Clinical trial applications and lifecycle management
Coordination with global regulatory teams
Labeling updates and regulatory database maintenance
Updating SOPs and safety agreements

🎓 Eligibility Criteria

B.Pharm / M.Pharm / Pharm.D
Life Sciences / Microbiology / Chemistry
Related healthcare disciplines

Experience Required:

Minimum 1+ year in Regulatory Affairs or Pharmacovigilance
Experience in pharma or biotech industry

⭐ Benefits of Working at Ferring

Global exposure in Regulatory & PV
Strong career growth opportunities
Family and wellness benefits
Paid parental and fertility support benefits
Collaborative global work environment

🎯 Interview Preparation Tips

Understand Indian regulatory submission process
Learn pharmacovigilance workflows (ICSR, PSUR)
Review ICH, GVP and CDSCO guidelines
Prepare basics of regulatory dossier preparation

Helpful resources:

📌 Note Before You Apply:
Kindly read the job description carefully before applying. Make sure your experience matches Regulatory Affairs & Pharmacovigilance requirements.