FDA approval in the tablet and capsule section is highly appreciated;* Minimum 5 years of hands on production experience Knowledge of various types of equipment of granulation, compression, coating, and capsule filling; Review Standard operating procedure of manufacturing equipment and…
This position is responsible for managing all cGMP aspects of Quality Assurance Operations of a WHO GMP approved Tablets and Capsule manufacturing facility. Specific Responsibilities: In Process Quality Assurance (IPQA) performing checks during manufacturing, such as sampling, manufacturing, packing, and…
Job responsibilities include below (but are not limited to) Gujarat FDCA approval in "Microbiological Assay/Limit Testing" section is a MUST To handle the microbiology department independently. Should be able to perform as per international regulatory compliance. Media Preparation Growing Microbe…