QC

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.

B.Pharm / M.Sc. - Review analytical & electronic QC data with tight QMS grip on incidents, OOS & OOT.

ITI / Diploma for Operators (Sterile USFDA Exp.) B.Pharm / M.Pharm for Officer (Sterile USFDA Exp.)

Execute routine & stability testing of pharmaceutical products. Ensure compliance with WHO-GMP, SOPs & regulatory requirements.

QMS & Audit Compliance: Implementation and maintenance of QMS, document control, internal audits, audit preparation, inspection support and CAPA follow-up.

Responsible for all IPQA activities, Qualification of Equipment, QMS, Equipment Qualification, HVAC Qualification, DRA Documentation

Pharmacopoeial standards for Biosimilars. Development and Characterization of Biosimilars. Biotherapeutics: Regulatory landscape

Experience in analysis of Solid Oral - FP, Instrumentation, In-process or Stability. Experience of Analytical Method Validation. Experience of PMQC & Dissolution. 

Shodhana Laboratories is a pharmaceutical company specializing in Active Pharmaceutical Ingredients (APIs) and Intermediates. Established in 2000, they cater to both generic and custom requirements for well-known pharmaceutical brands