Strong understanding of OSD manufacturing processes and knowledge of cGMP and relevant regulatory requirements. Candidate should have good exposure to QC instruments HPLC/ GC/ LCMS, Dissolution, UV Spectrophotometer/ KF/ Autotitrator / Malvern analysis and trouble shooting
To ensure timely completion of analysis and data completion for the same. To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental quality systems. M.Sc / BPharm or any relevant degree
Exposure to OSD Manufacturing operations like Granulation, Compression, Pellet coating, Capsule filling, Primary Packing and Secondary Packing. Expertise in e-BPR and e-log will be added advantage. Experience in analysis of Solid Oral - FP, In-process or Stability samples. Experience of HPLC, UV spectrophotometer and Dissolution Tester operation. Experience of Analytical Method Validation/Transfer Solid Oral. Experience of GC, ICPMS and/or LCMS operation.
Gufic Biosciences Ltd is a leading pharmaceutical industry since 1970 and is one of the world’s largest Lyophilization injectables & wide range of API products, at Navsari (Gujarat). International accreditation of WHO, GMP, EU, Canada, Russia, Anvisa, etc.
Collaborate with outsource parties to full fill laboratory requirement in timely manner. Previous experience in analytical method validation would be an added advantage.
B. Pharma. /B.Sc. Biotech./B.Sc. Medicinal Chemistry/B.Sc. Pharmaceutical Chemistry M.Pharma/M.Sc. Biotech /M.Sc. Medicinal Chemistry /M.Sc. Pharmaceutical Chemistry. To assist in preparation of purchase orders and send copies to suppliers and to departments originating requests. Follow up with suppliers in respect of timely supplies of products with respect to the issued purchase orders.
Granules India is a vertically integrated, high-growth pharmaceutical company with 38 years of proven performance and increasing performance and increasing presence across the world. Headquartered in Hyderabad, India, Granules offers collaborative and strategic partnership to global pharmaceutical leaders by producing best quality API, PFI and FD through manufacturing excellence, process innovation and regulatory expertise.
Oversee daily QC laboratory operations, ensuring compliance with cGMP, FDA, and other regulatory requirements. Validate, and implement analytical methods, including HPLC and plate-based assays as well as General assays. Ensure accurate and timely testing of raw materials, packaging materials, in-process samples, and finished products.
SCIENCES, PHARMACY GRADUATES B.SC, M.SC, B. PHARM, M. PHARM WITH 0 TO 3 YEARS EXPERIENCES IN ANY OF QA FUNCTION VALIDATION, IPQA, QMS, COMPLIANCE, DQA, LAB QA OF A FORMULATION - STERILE, NON STERILE DOSAGE