Follow shift schedule and production schedule. Compliance to all approved procedure, documents and GMP activities.
Perform all the assigned production activities in confirmation to Batch record, protocols and recording the details in record sheets and log books.
Execution of Routine EMP and updating the data in ISEM portal. Preparation of the investigation reports for the EMP excursions and deviation.
Co-ordinate with Sterility Assurance if any ISEM related user access request in suite. Preparation of trends for investigation purpose.
Taking trends from BI tool. Maintain 5S in Office-2. Archive NVPC reports to QA documentation. Maintain process and facility related Documentation. Coordination with media and technical services personnel to avoid delays.
Update PRP and PRP-T data in Citrix. In case of any abnormalities/ deviation observed should be recorded and informed to process in-charge to avoid any quality issues in the product.
Experience: 3 - 5 Years
Qualification: M.Sc (Bio tech / Microbiology / Bio Chemical) / B.Tech Biotech
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
Keyskills: Biotechnology Assurance Process Incharge Technical services Microbiology Diversity and Inclusion Investigation EMP Production scheduling GMP
Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the...