Sciences or Pharmacy Graduates with 3 to 8 years Experiences in parenteral vial , ampoules, bottles of glass or Plastic through, BFS technology. Candidate worked in production compliances, remediation, and having experiences of managing quality system document
Experience in testing of finished products, LST and stability samples. Preferably worked in FDA Approved organizations. Hands on knowledge of cGMP, GLP, 21 CFR and any other regulatory requirements.
Responsible for identifying and driving improvement projects within Deviations, CR handling, and other relevant processes, together with the process manager. Derive KPIs for the QMS and measure performance and put in place improvements.
Experience in OSD Manufacturing Plant is must. Candidates should have knowledge of cGMP, hands on experience in packing Blister and Bottle, initiating QMS activities and should have experience to regulatory audits.
Having Injectable Experience of Analysis of raw material, In-process, Finish products, Stability testing, Process validation. Hands on Experience of HPLC, GC, LBPC, Osmometer, KF Auto titrator and UV - Visible spectrometer.
Morepen are a leading pharmaceutical company dedicated to improving health and well-being through innovative medicines and healthcare solutions. We are looking for a motivated and dynamic Officers to join our team and contribute to our mission of delivering high-quality healthcare products.
Candidates must have hands on experience to perform line clearance activity before commencing the different operations like dispensing, filling, inspection, sealing, packing.