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.
QC Micro Department
Qualification : M.Sc. (Microbiology / Biotechnology)
Post : Executive / Sr. Executive
Experience : 3 to 6 years
Key Skills : • MLT Analysis & Validation
• Water analysis and validation
• Cultura Handling & identification
• QMS & Documentation
• Good Instrument Handling
QC Department
Qualification : M.Pharm / M.Sc.
Post : Executive
Experience : 3 to 5 years
Key Skills : • Raw material analysis and finish product analysis
• Stability analysis
• Preparation of departmental SOP & validation protocols in compliance with current guidelines
QC Department
Qualification : M.Pharm / M.Sc.
Post : Sr. Executive
Experience : 4 to 6 years
Key Skills : • Planning & Execution of analysis of finish product
• Performing raw material testing
• GLP activity
• Daily / monthly calibration & PQ of instruments / equipment.
Job Location : Plant (Sakodara Village), Ahmedabad
Apply to hr@apdmpharma.com
OR
Last Date : 30th May 2024
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