FULL TIME Educational Qualification BTech/MTech/MSc Experience Minimum of 15 Years of Experience in Cell Culture Upstream Process Job Description To lead Upstream team in Drug Substance Manufacturing Department. To provide guidance and train the sub ordinates. To Ensure cGMP principles are followed by team members. Responsible to Prepare / review protocols, reports, Batch Manufacturing Records, Standard Operating Procedures and Qualification Documents. To comply with National and International quality and regulatory standards and always be ready for all kinds of internal and external audits.

FULL TIME Educational Qualification BTech/MTech/MSc Experience 6-8 Years in experience in Mammalian Cell Culture Upstream Processing in Manufacturing Department Job Description Responsible to manage the vial thaw, cell counting, seed expansion activities. Responsible to manage media preparation, wave bioreactor, SS bioreactor operations. Responsible to maintain documentation activities like - Batch Manufacturing Records/Special Process Requirements. Responsible in maintaining Quality Management Systems related documentation like deviations, change controls, risk assessment documents etc. Responsible to manage the facility maintenance as per cGMP guidelines.