QA

Conduct audits across bioanalytical and statistical study phases to ensure compliance with study protocols, SOPs, GLP, GDP, SOPs, and applicable regulatory requirements.

Doc-cell (Document Control. BMR/BPR Issuance, SOP Management, Controlled Copy, Change, Archival, Audit Support)

Exposure of water HPLC, Dissolution. GC and other Instruments with AMV. RM, PM, FP product analysis. GLP

B.Pharm or Graduation in Biomedical Sciences. Minimum 3 years experience for Operations Manager and 1 year experience for Associate Manager in pharmaceutical / medical device regulatory affairs.

HPLC & GC operation Empower Software Wet Lab Analysis UV IR SOR LOD AIT KF BD FTIR PSD SA etc. Automated instrument operation. Mankind Pharma Interview, M.Pharm, B.Pharm, M.Sc, B.Sc

B.Pharm | M.Pharm | B.Sc | BA | ITI | D.Pharma B.Com | M.Com, Ipca Labs

Liquid filling, Packing, Compression, Granulation, Capsule Filling, Coating & Encapsulation

Review analytical documents, raw data, STPs, and laboratory records to ensure compliance with cGMP and regulatory requirements. Hetero, B.Pharm, M.Pharm, M.Sc Chemistry  Apply

M.Pharm, B.Pharm, M.Sc, B.Sc, D.Pharm, ITI, B.E, B.Tech jobs at Titan Laboratories Pvt. Ltd. and Titan Pharmaplus Pvt. Ltd. are holding a walk-in interview drive for their Formulation and API plant located in Mahad (Raigad).