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

QA Department
Post & Qualification : Officer / Sr. Officer (M.Sc./ M. Pharm)
Experience : 2 to 4 years
Skills : To support regulatory licensing activities by preparing documents, tracking approvals, and ensuring compliance with pharmaceutical regulatory requirements, Assist in preparation and submission of documents for CDSCO, State FDA, DSIR, and WHO-GMP approvals, Support applications for manufacturing licenses, import licenses, and test licenses for R&D and plant operations, Maintain and update regulatory license records, including application status, approvals, and validity dates, Support compliance with Drugs & Cosmetics Act, Rules, and applicable regulatory guidelines.

TT Department
Post & Qualification : Officer / Sr. Officer (B.Pharm / M.Sc.)
Experience : 0 to 2 years
Skills : Develop and maintain documentation for pharmaceutical products, including Specifications , Standard Testing Procedures & Test Data Sheets To create, manage, and maintain comprehensive documentation for our pharmaceutical products.

ADL Department
Post & Qualification : Officer / Sr. Officer Executive / Sr. Exe. (M.Sc./B.Sc./ M. Pharm)
Experience : 2 to 6 years
Skills : 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.

FD Department
Post & Qualification : Officer / Sr. Officer Executive / Sr. Exe. (M.Pharm)
Experience : 2 to 6 years
Skills : Development of simple and complex parenteral & ophthalmic formulations – Generic & 505(B)(2), Conduct literature research and evaluate new technologies/excipients, Preparation of documents like MFR, PDR, Protocols, SOP & other Tech Transfer documents, Support scale-up, exhibit batches & tech transfer, Collaborate with Analytical, QA, RA & Production teams.

Job Location : R&D Unit, Changodar 

Walk in Interview
Date : 30 & 31st January 2026
Time : 08:30 am to 04:30 pm
Venue : Unit No. 90 & 91, Parishram Industrial Hub, Chacharwadi – Vasna, 
Changodar, Ahmedabad, Gujarat-382213.

Pls bring Resume and one passport size photo