Tashi Pharma is urgently hiring a Regulatory Affairs Executive in Ahmedabad, offering an excellent opportunity for freshers and early-career professionals (0–1 year experience). If you hold a B.Pharm or M.Pharm degree and are looking to build a career in pharmaceutical regulatory affairs, compliance, and documentation, this role is ideal.
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This position focuses on handling regulatory submissions, WHO GMP certifications, product permissions, and licensing activities, making it a strong entry point into global regulatory operations.
💼 Key Responsibilities – Regulatory Affairs Executive
- Handle application and management of Loan Licences, including maintenance and renewals
- Prepare and submit Product Permission applications and Certificate of Pharmaceutical Product (CoPP)
- Coordinate WHO GMP certification applications with FDCA and ensure timely renewals
- Track renewal schedules for Manufacturing Licenses and regulatory certificates across sites
- Apply for No Objection Certificates (NOC) and ensure regulatory compliance
- Manage documentation for Apostille, Notarization, Legalization, and Embassy attestation
- Maintain and manage retain samples and commercial samples as per regulatory norms
🎓 Qualifications Required
- B.Pharm / M.Pharm (Pharmacy graduates preferred)
- 0–1 year experience in Regulatory Affairs / Pharma Compliance
- Basic understanding of WHO GMP, FDCA regulations, and documentation processes
- Strong attention to detail and documentation skills
🎁 Benefits & Career Growth
- Excellent opportunity for freshers in Regulatory Affairs
- Hands-on exposure to global regulatory submissions and compliance
- Work with experienced professionals in pharma licensing and certification
- Career growth in Regulatory Affairs, QA, and international submissions
📩 How to Apply
Interested candidates can apply by sending their updated resume to:
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