Regulatory Affairs Job at Ferring Pharmaceuticals | Life Sciences | Apply Now
Ferring Pharmaceuticals is inviting applications for the position of Executive – Regulatory Affairs & Pharmacovigilance at its Mumbai location. This dual-function Regulatory Affairs Job is essential for managing the product lifecycle and safety reporting across the India and South Asia cluster (India, Sri Lanka, Bangladesh, etc.). This Lifesciences Job offers an integrated experience in both pre-market regulatory submissions and post-market safety monitoring within the pharmaceutical and biotech industry.
- Job Position: Executive (RA & PV)
- Job Requisition ID: R0035732.
- Location: Mumbai, India (Ferring India M&S).
About the Company
Ferring Pharmaceuticals is a research-driven, specialty biopharmaceutical group committed to helping people build families and live better lives. With a strong presence in Reproductive Medicine, Maternal Health, and Gastroenterology, Ferring offers a dynamic environment for RA and PV professionals to manage critical health portfolios across South Asia.
Key Responsibilities & Functional Scope
The role requires navigating complex local and cluster-level regulations while maintaining global safety compliance standards.
Regulatory Affairs (RA) Duties
- Dossier Management: Preparation of dossiers for new products, clinical trials, variations, and renewals for Indian and South Asia regulatory authorities.
- Authority Interaction: Coordinating query responses and contributing to preparations for Regulatory Authority and Expert Committee meetings.
- Commercial Support: Reviewing promotional materials for registration compliance and ensuring timely updates for the National Pharmaceutical Pricing Authority (NPPA) database.
- Lifecycle Maintenance: Updating labeling materials, maintaining regulatory databases, and informing commercial teams of major milestones.
Pharmacovigilance (PV) Duties
- Safety Reporting: Reporting safety information to Global Safety teams and conducting follow-ups with reporters for additional data.
- Compliance Tracking: Performing monthly reconciliation, compliance checks, and submitting Periodic Safety Update Reports (PSURs) as per local regulations.
- Safety Agreements: Updating and renewing Safety Agreements for partners, manufacturers, and distributors.
Eligibility & Experience Profile
This Pharmacovigilance job is designed for early-career professionals with a strong foundation in pharmacy or allied sciences.
- Educational Background: Bachelor’s in Lifesciences or Microbiology.
- Required Experience: Minimum of 1+ years in India Regulatory Affairs and Pharmacovigilance functions within the Pharma or Biotech industry.
- Technical Knowledge: Familiarity with local SOPs, safety mailbox management, and Indian regulatory guidelines for clinical trials and product renewals.
- Core Focus: Regulatory dossiers, labeling, Pharmacovigilance (PV) reconciliation, and pricing authority (NPPA) coordination.
Advancing your career with a Regulatory Affairs Job at Ferring provides a comprehensive platform to master both market access and patient safety. This Lifesciences Job in Mumbai is an ideal progression for professionals who want to lead dossier preparations and Pharmacovigilance job workflows across multiple South Asian countries. If you have the required pharmaceutical background, ensure you apply via the Ferring careers portal.
