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1.0 - 8.0 years
0 Lacs
ahmedabad, gujarat
On-site
You will be responsible for managing the Quality Management System (QMS) for drug substance of bacterial products. It is essential to have a solid understanding of the process involved in both upstream and downstream unit operations. Your role will involve handling QMS documents including deviations, change controls, and investigations using Track-wise software. In addition, you should have experience in ensuring audit compliance, adherence to regulatory guidelines, and proficiency in documentation such as Standard Operating Procedures (SOPs) and Batch Manufacturing Record (BMR) preparation. This position requires a minimum of 5-8 years of experience in QMS, compliance, and documentation, with a strong understanding of manufacturing process operations related to bacterial and recombinant vaccines, as well as biological therapeutics.,
Posted 5 days ago
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