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Career Opportunities at APDM Pharmaceuticals in Quality and Production Operations

Opportunities Await for BPharm, MPharm, MSc in QC, QA, Production / Packaging at APDM Pharmaceuticals

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.

WALK IN INTERVIEW

Quality Control
Post : Trainee / Sr. Officer / Executive / Sr. Executive 
EU, MHRA, USFDA & ANVISA audits/ regulatory exposure is MUST required.
Qualification : M.Sc./M.Pharm /B.Pham
Experience : 0 to 6 Years
• RM Sampling & Analysis (Chemical & Instrumentation) HPLC, GC, IR, KF, UV, POLARIMETER, Dissolution Chemical Testing, FP/IP/Stability Analysis (Chemical & Instrumentation), Planning of AMT, AMV, API verification & Review, overall GLP maintaining & compliance, Preparation of MOA and protocols. Coordination for TT & AMV, Must have knowledge of cGMP, GLP, ALC00++ principle & GDP. Experience in Document preparation and review is MUST.

Quality Assurance
Post : Officer / Sr. Officer / Executive 
EU, MHRA. USFDA& ANVISA audits/ regulatory exposure is MUST required.
Qualification : M.Sc./M.Pharm /B.Phanm
Experience : 2 to 7 Years
IPQA, Vendor Qualification, Technology Transfer, QMS, Validation, Qualification, Documentation Quality Risk Assessment


Production / Packaging
Post : Sr. Officer / Executive 
EU, MHRA. USFDA & ANVISA audits / regulatory exposure is MUST required
Qualification : M.Sc./M.Pharm /B.Pharm
Experience : 3 to 7 Years
• BMR, BPR, SOP preparation
• Change Control Management. Deviation Management, Quality Risk Assessment
• Audit readiness & compliance
• Coordination with cross functional team
• Line clearance / logbook entry, BMR, BPR entry
• Vendor Qualification

Quality Assurance
Post : Manager / Sr. Manager
EU, MHRA, USFDA& ANVISA audits/ regulatory exposure is MUST required.
Qualification : M.Sc./M.Pharm /B.Pharm
Experience : 10 to 15 Years
• IPQA
• Vendor Qualification
• Technology Transfer
• QMS, Validation
• Qualification
• Documentation
• Computer System Validation
• Quality Risk Assessment & compliance


Job Location : Plant, Sakodara

Walk in Interview
Date : 7th February 2026
Time : 09:30 am to 05:00 pm
Venue : 403, Patron, Opp. Kensvilla Golf Academy, Rajpath Club Road, Bodakdev, Ahmedabad

Pls bring Resume and one passport size photo

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