APDM Pharmaceuticals Private Limited has its office in Ahmedabad with all QA and regulatory support staffs for managing CDO and CDMO projects ,vendor Audits, BA BA monitoring, project and Engg team. We are a global pharmaceutical service providers with a vast global network of CMO’s, CDMO’s and CRO’s. We have more than 100 years of CDMO, 50 years of R&D and decades of regulatory and QA experience in our company.
APDM Pharmaceuticals Private Limited is inviting applications for Executive / Sr. Executive - Regulatory Affairs to join our growing team at Ahmedabad (Head Office).
Post : Regulatory Affairs Specialist
No of posts : 02
Experience : 4-6 years
Qualification : B.Pharm / M.Pharm
Key Responsibilities
• Dossier preparation & submissions (US, EMEA mandatory)
• Regulatory compliance & query handling
• Documentation & record management
• Cross-functional coordination
• Regulatory updates & intelligence
• eCTD and labeling will be added advantage
OFFER
1nd & 3rd Saturday Off
Attractive HR Policies
INTERESTED CANDIDATES MAY SHARE THEIR CV AT : career@apdmpharma.com
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