Candidate must have extensive experience in pharmaceutical production operations with strong knowledge of CMP, team handling, production planning, documentation, and coordination with QA / QC.
Candidate must have strong hands-on experience in QMS activities including Deviation, CAPA Change Contol, OOS handling. SOP documentation, and regulatory audit support in injectable / parenteral manufacturing.
Experience in analysis in HPLC / GC, Qualification / Re-Quaiification of Laboratory instrument(DQ/IQ/OQ/PQ), Preparation of AMV protocol. Responsible for QMS activity like : CCP, Deviation, OOS, OOT, UR.
Post Graduate Degree MSc Life Science / MPH / MHA / M.Pharma (Master of Pharmacy) / Pharm.D (Doctor of Pharmacy) with 4 years of experience in relevant area
M.Sc. degree in Biochemistry, Microbiology, Biotechnology, or Genetics with a first-class academic record. Candidates with a minimum of two years of research experience in tuberculosis will be preferred. Applicants must have qualified NET or GATE.