Royal Pharmaceuticals Industries Pvt. Ltd. for experienced professionals in Regulatory Affairs (RA). If you have 2+ years of experience in pharma regulatory functions, this could be your next career move.
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This Regulatory Affairs job in Boisar offers a chance to work in a growing pharmaceutical company and gain exposure to regulatory submissions, compliance, and documentation.
Job Details
- Company: Royal Pharmaceuticals Industries Pvt. Ltd.
- Position: Regulatory Affairs (RA)
- Location: Boisar, Maharashtra
- Experience: Minimum 2 years
- Industry: Pharmaceutical
Key Responsibilities (Regulatory Affairs RA Jobs)
- Prepare and review regulatory submissions (CTD/eCTD dossiers)
- Handle product registration documentation for domestic and international markets
- Ensure compliance with regulatory guidelines (CDSCO, WHO, ICH)
- Coordinate with cross-functional teams for regulatory approvals
- Maintain updated records of regulatory filings and licenses
- Assist in audit preparation and responses
- Monitor changes in regulatory requirements and implement updates
Qualifications Required
- B.Pharm / M.Pharm / Life Sciences Graduate
- Minimum 2+ years experience in Regulatory Affairs (RA)
- Strong knowledge of pharma regulatory guidelines and documentation
- Experience in CTD/eCTD submission preferred
- Good communication and documentation skills
Salary & Benefits
- Estimated Salary: ₹3.5 LPA – ₹6.5 LPA (based on experience)
- Opportunity to work in regulatory affairs domain
- Exposure to global regulatory markets
- Career growth in pharmaceutical compliance & submissions
Why Join Royal Pharmaceuticals?
- Growing pharmaceutical organization
- Hands-on experience in Regulatory Affairs jobs in India
- Opportunity to work on global submissions & compliance
- Professional development in regulatory domain
How to Apply
Interested candidates can apply by sending their updated resume to:
📧 Email: sonampawar@royalpharma.in
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