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B.Pharma / M.Pharma/ B.Sc / M.Sc. (Organic Chemistry / Analytical Chemistry); experience in injectable manufacturing, Aseptic area operations, Packing, Visual inspection, QMS activities. relevant functional experience in OSD manufacturing and Packing operations / QMS activities

B.Pharma, B.Sc., M.Sc.  Granulation, Compression, Coating, Continuous coater, Capsulation, Press-fit, Inspection. Blister Packing, Bottle Packing, Bulk Packing. Exhibit/IP/FP, Hold Time, Stability, Vendor Qualification, Method Validation and GLP, RM, PM, VQ, Sample Management

Masters degree in Life Science, or equivalent with at least 60% marks. Experience in IP management, patent drafting, certification in IPR will be preferred. Prior art search, good organizational skills, strong written and verbal communication skills and basic computer knowledge are desirable.

Formulation development in solid orals tablets, Capsules, Pellets, Soft gels. Should have experience in extended release, delayed release, multiparticulate.

Manufacturing, filtration, filling, Lyophilization, sealing, and pre- and post-manufacturing activities. Planning and execution of batch manufacturing activities, filling activities, lyophilization, sealing activities, and filter integrity. Monitoring NVPC and trending.

M. Pharma / B. Pharma; Awareness of regulatory requirement, ANDA filing & new Product filing application, Handle Field Alert Report, Market complaint, Review & presentation of Data, Tracking of data. Planning for sample pullout, Batch charging, storage & reconciliation, destruction & smooth functioning of Stability chamber, Walk-in Chamber

Conduct QC testing on raw materials, packaging, stability, in-process, and finished products. Capable of Handling Instrument like HPLC, GC,KF, IR,UV instrument. To review analytical data & handling of QMS i.e. Deviations, 00S, 00T, Laboratory incidences, OOC, CAPA and Effectiveness of CAPA.

Monitor and supervise production process to ensure compliance with SOP and cGMP. Maintain documentation as per regulatory authorities requirement like change control, deviations. Highlight technical problems and take corrective actions.