Regulatory Affairs Jobs at Ferring | BSc Chemistry Graduates Apply Now
Are you looking for Regulatory Affairs Jobs or Executive Jobs in the pharmaceutical industry? This Executive – Regulatory Affairs & Pharmacovigilance position in Mumbai is an excellent opportunity for professionals seeking to build a strong pharmacovigilance career, including candidates exploring BSc Chemistry Jobs and life sciences roles within a globally recognized pharma organization.
About Ferring
Ferring India M&S is part of Ferring Pharmaceuticals, a global, research-driven biopharmaceutical company operating in more than 50 countries. The company focuses on developing and delivering innovative therapies in reproductive medicine, gastroenterology, and urology. With a strong commitment to patient safety, quality, and regulatory compliance, Ferring offers excellent opportunities in Regulatory Affairs Jobs, Executive Jobs, and a long-term pharmacovigilance career. In India and South Asia, Ferring supports regulatory submissions, safety reporting, and product lifecycle management, making it an ideal workplace for pharmacy and life sciences professionals, including candidates seeking BSc Chemistry Jobs in the pharmaceutical industry.
- Position: Executive – Regulatory Affairs & Pharmacovigilance
- Location: Mumbai, India
- Job Requisition ID: R0035732
Qualification: Bachelor’s in Pharmacy or Lifesciences or Microbiology, Chemistry, or similar
Experience: 1+ years in India Regulatory Affairs and Pharmacovigilance functions in the Pharma
or Biotech IndustryJob Description:
- Reporting of safety information: From India & India cluster (South Asia countries) to the Global Safety
- Follow-up: For additional information with the reporters
- Review the safety mailbox: For the reports
- Monthly Reconciliation and Compliance checks: From the PV perspective
- Submission of Periodic Safety Update Reports: To the regulatory authority as per regulations
- Dossier preparation: Gathering requirements and preparation for Indian regulatory authority submissions, including new products, clinical trials, variations, renewals, and query responses. Coordinate with global teams.
- Regulatory authority preparation: Contribute in preparation for meetings and expert committee meetings
- Labeling materials preparation and updates: For our products
- Promotional material review: To ensure compliance with product registrations
- Regulatory Databases: Timely information for updation
- SOP updates: Updation of local SOPs
- Safety Agreements: Updation/renewal for Partners, Manufacturers, Distributors
- Price updates coordination: Checks for price updates and timely data entry into the Pricing Authority database (NPPA)
- Lifecycle maintenance and updates: Update the commercial team on major milestones
