QC

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

B.Pharm / M.Pharm / M.Sc. (Chemistry or Analytical Chemistry) ; experience in a WHO-GMP compliant pharmaceutical Quality Control laboratory. Taj Pharma India

B.Pharm / M.Pharm / M.Sc . Expertise in analysis on HPLC, GC, Assay, Dissolution. Method Validation Protocol creation and execution, Expertise in handling HPLC, ICPMS, GC etc. USV Private Limited