Ferring Pharmaceuticals, a globally recognized biopharmaceutical company, is inviting applications for the position of Senior Executive – Regulatory Affairs at its Hyderabad R&D center. This is an excellent opportunity for experienced regulatory professionals to work on global submissions, pharmacovigilance, and compliance in a dynamic environment.
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📌 Job Overview
- Role: Senior Executive – Regulatory Affairs
- Location: Hyderabad
- Job Type: Full-Time
- Experience: Minimum 5 Years
- Qualification: M.Pharm
- Application Deadline: May 20, 2026
- Job ID: R0037249
🚀 Key Responsibilities
As a Regulatory Affairs professional, you will:
- Manage regulatory submissions and pharmacovigilance case processing within timelines
- Prepare, review, and compile dossiers for Marketing Authorization (MA) in India
- Handle submissions such as:
- CDSCO NOCs, BE NOC applications
- Import permissions and product/site registrations
- Apply for regulatory certifications:
- GMP, GLP, COPP, FSC, WHO-GMP, EU WC
- Conduct gap analysis and risk assessments for regulatory submissions
- Coordinate with CROs and CMOs for timely submissions
- Support new product development with regulatory strategies
- Review:
- Protocols, validation plans, reports, DMFs, artworks, and CMC documents
- Respond to regulatory authority queries effectively
- Ensure global regulatory compliance and internal policy alignment
🎓 Qualifications & Skills
- Education: M.Pharm (Mandatory)
- Experience: Minimum 5 years in Regulatory Affairs
- Strong expertise in:
- Indian and global regulatory frameworks
- Dossier preparation and submission processes
- CDSCO regulations and documentation
- Ability to handle cross-functional coordination and deadlines
💼 Benefits & Career Growth
- Opportunity to work with a global pharmaceutical leader
- Exposure to international regulatory markets
- Career advancement in R&D and regulatory strategy
- Collaborative and innovation-driven work culture
📩 How to Apply
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