Experience must include analysis of Raw Material, In-Process, finished goods; Stability Testing & Stability sample handling for Tablets, Capsules Handling of HPLC, dissolution & other sophisticated instruments.
Graduate in Science Physics, Chemistry, Botany, Zoology, Life Science, Pharmacy with Degree, Diploma in Clinical Research. Minimum 1-year experience in Clinical Research, Ethics committee, Monitoring
Hetero Drugs is an Indian pharmaceutical company and the world’s largest producer of anti-retroviral drugs. Hetero’s business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics. Globally renowned, vertically integrated pharmaceutical player engaged in Research and Development (R&D), manufacturing, and marketing of high-quality chemical and biologic medicines across diverse therapeutic areas.
B.Pharm, M.Sc, M.Pharm with 3-8 years of experience in IPQA and manufacturing, packing QMS related activities in oral solid dosage form tablets, capsules, soft gelatin capsules, pellet Dosage form manufacturing facilities.
Can handle instrument i.e HPLC- Dissolution 3C, IR,UV, QC QMS, Material testing xposure on EM, water testing, MLT testing of FP and RM/Stability samples , Analysis and review of Micro samples, reports.
Having Injectable Experience of Shop floor Supervising activities like Aseptic Filling, Autoclave Operations, Compounding vessels operations, Manpower Planning, Change Controls, investigations, CAPA, Vial Washing, Lyophilizers and Training and QMS
Endo India Par Formulations is a pharmaceutical company that develops, manufacturers and markets safe, innovative and cost-effective pharmaceuticals that help improve patient quality of life. At Endo our investment in state-of-the-art equipment and facilities, commitment to ethical standards, and growing portfolio of products makes us a company where you can enjoy a productive career with long-term potential.
Exposure of handling and compliance of various compression, coating and granulation machines, equipment Online documentation of BMR and log books during execution of batches.