To perform line clearance activity before starting of different operations like dispensing, manufacturing, filling, inspection, sealing, labeling & packing.
Experience in API Production, Bulk Drug, API Production To be responsible for Batch start up activity, monitoring, calibration of balance and other instruction given by the Superior, Should have exposure in reactors, centrifuges, and a clean room equipped with sound knowledge in cGMP and SOPs.
Ph.D. in relevant discipline and M.Pharm Pharmaceutical Quality Assurance, experience and good track record of publications, patents. The candidates who have submitted PhD thesis may also apply.
The individual has experience in handling various analytical techniques such as such as HPLC, GC, CE-SDS, SEC, ELISA, qPCR, DSC, Bioassay, Karl Fischer, UV, LC-MS, Dissolution, Disintegration, X-ray diffraction, etc.
Masters degree in pharmacy, life sciences, biotechnology is required. At least 1 year in healthcare company analysis, market research, or US market access, knowledge of US healthcare marketplace and government programs such as Medicaid, Medicare etc
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.
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.