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APDM Pharmaceuticals Opens Roles in Quality Control and Quality Assurance

APDM Pharmaceuticals Opens Roles in Quality Control and Quality Assurance

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

Executive / Sr. Executive
EU, MHRA, USFDA & ANVISA audits/ regulatory exposure is MUST required.
Dept : Quality Control
Exp : 4 to 6 years
Skills : • 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.

Officer / Sr. Officer / Executive
EU, MHRA, USFDA & ANVISA audits / regulatory exposure is MUST required.
Dept : Quality Assurance
Exp : 4 to 6 years
Skills : IPQA, Vendor Qualification, Technology Transfer, QMS, Validation, Qualification, Documentation

Job Location : Plant, Sakodara


Walk in Interview
Date : 20-01-2026
Time : 08:30 AM to 03:30 PM
Venue : Plot No. 775,776 & 628, Vill.: Sakodara, Taluka Bavla, Ahmedabad, Gujarat-382220

Pls bring Resume and one passport size photo.


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