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.
Post : Officer / Sr. Officer / Executive / Sr.Executive - QC (Documentation & Method Validation)
Job Description
• Perform and review method validation of Assay, Dissolution, Related compound and Residual solvents etc.
• Preparation of method validation/verification protocol (API and finish product).
• Preparation of STPs and Specifications as per method validation protocol.
• Check the method transfer protocol/report and methods and resolve the query of Assay, Dissolution, Related compound, Elemental analysis and Residual solvents etc.
• Ensure timely completion of validation/verification and method transfer.
• Check all availability like the column, Impurities, reference standard, chemicals and reagents etc. as per MOA/Protocol for exhibit batches analysis/validation/Verification.
Additional Information
Education : M.Sc / M.Pharm
Experience : 2 to 5 years
Job Location : Plant (Sakodara VitL, Ahmedabad)
End Date : 10th February 2025
Apply to hr@apdmpharma.com
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