Team member -Drug product

• Team member responsible for buffer preparation & Formulation operation as per SOPs, Batch Production Record and cGMP procedure.
• To Work in shift operation as per production schedule.
• To ensure all documents related to FFM such as status label updation, on time completion of BPR, area / equipment log books, RSTs updation & archival.
• To Execute & review batch production record & responsible to address the QA review comments of the BPR within TAT
• To carry out all batch related SAP transactions like SAP Confirmation.
• To ensure disinfectant preparation, filtration, reconciliation and to ensure the consumable stock as per requirement.
• To ensure the area & equipment cleaning of FFM facility as per schedule.
• To carry out & verify consumable & Raw material dispensing / issuance from the warehouse & to verify the MRN of the left over material to Warehouse.
• To coordinate & assist CFT to comply scheduled PM, Calibration & validation activity of the equipment & area in FFM facility.
• To ensure & assist manufacturing facility modification & maintenance.
• To ensure timely & accurate reporting of the discrepancies related to production operation & to participate in its investigation & CAPA implementation.

Apply Link- Apply Link mentioned in below

We are committed to providing access to affordable and innovative medicines, driven by our purpose of Good Health Cant Wait.Our products and services are spread across our core businesses of Active Pharmaceutical Ingredients (API), generics, branded generics, biosimilars and over-the-counter pharmaceutical products around the world. We work towards meeting unmet patients needs in the areas of gastro-enterology, cardiovascular, diabetology, oncology, pain management and dermatology. We are investing in businesses of the future including drug discovery, clinically-differentiated assets and digital healthcare.