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
EU, MHRA, USFDA & ANVISA audits / regulatory exposure is MUST required.
Qualification : M.Sc. / M.Pharm
Job Location : Plant (Sakodara Vill., Ahmedabad)
Officer / Sr.Officer (Total 4)
Experience : 2 to 5
Skills / Brief profile : Packing material, UV, IR, KF, Polarimeter, Titration and Chemical Analysis, Knowledge of sampling and release of packaging material, Preparation of SoP, Specifications (RM/PM/IP/FP/Stability), MOA, Protocols, GTP, Training, Method Transfer, Method Verification, API Verification and Documentation Work.
Executive / Sr. Executive (Total 5)
Experience : 4 to 6
Skills / Brief profile : RM Sampling & Analysis (Chemical & Instrumentation) HPLC, GC, IR, KF, UV, POLARIMETER, Dissolution Chemical Testing, FP/IP/Stability Analysis (Chemical & Instrumentation)
Sr. Exe. / AM / Manager / Dy. Manager (Total 2)
Experience : 6 to 12
Skills / Brief profile : 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
Analytical Development
Qualification : M.Sc. / M.Pharm
Job Location : R&D Unit, Changodar
Officer / Sr. Officer/Executive/Sr. Executive Total - 06
Experience : 0 to 8
Skills / Brief profile : • To Perform Analytical Method Development of Assay, Dissolution, Related substance & other test for Drug Products.
• Perform, Analytical Method Validation, Analytical Method Verification and Analytical Method transfer.
• To perform the of Multimedia Dissolution profiles, R&D stability analysis & Plant support for investigation study.
• Preparation of STP and Specification for Drug Product, Drug substance and excipient.
• Preparation of Protocol and Report for Analytical Method Validation/verification/Transfer. Maintained the Raw data for performed analysis as per GDP/GLP.
Walk in Interview
Date : 15-11-2025
Venue : 403, Patron, Opp. Kensvilla Golf Academy, Rajpath Club Road, Bodakdev, Ahmedabad (Time 09:30 am to 04:30 pm)
Unit No. 90 & 91, Parishram Industrial Hub, Chacharwadi - Vasna, Changodar, Ahmedabad, Gujarat-382213. (Time 09:00 am to 04:30 pm)
Pls bring Resume and one passport size photo.
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