Executing chemical reactions in mg to gm scale and to synthesize required quantities of molecules/ compounds as per client specifications using efficient route and techniques
Hands-on experience in handling the complete life cycle from review, submission and queries to post approval of Topical, Dermatological Formulations. Adherence to high quality, and regulatory standards in dossiers.
M.Pharm, B.Pharm, M.Sc. LLS has following openings for its EU-GMP Approved Global Standard OSD & Semi-solids Formulation manufacturing facility at Akola.
PRINCIPAL in Pharmacy Professor and 15 years of academic experience, including 5 years of administrative experience as HOD; We invite a fresher PhD with an excellent research area.
M.Pharm / M.Sc; A thorough knowledge related to development, and analytical troubleshooting for Ophthalmic, Injectables and NDDS formulations. In-depth analytical knowledge of techniques and operations viz HPLC, GC, LCMS, PSD, IVRT, Extractable-Leachable.
Batch Disposition post reviewing the batch manufacturing, packing, and testing records assuring compliance with established SOPs, specifications, and standard formats and ensures that all investigations related to batch are closed prior to the batch disposition.
Experience in reviewing specifications and STPs, ensuring data integrity, proposing QbD Quality by Design process changes, and participating in phase gate reviews
Candidate should have knowledge of manufacturing operations of granulation, compression, coating and capsule filling, responsible to adherence cGMP guidelines. USFDA, MHRA exposure is must.