Posted Date 20 Sep 2025 Function Business Area Life Sciences Location DALC - Navi Mumbai Job Responsibilities To ensure manufacturing as per SOP and timely completion of projects 1 Plan Execution of product manufacturing To facilitate Operation changeover of process systems debottlenecking of process hurdles Regular interaction with Operation team QAD and supporting functions to achieve the desired targets Focus on plant goals in order to attain expected products over all batch yield Coordinate and monitor the manufacturing schedule to ensure proper utilization of process units utilities etc Hands on experience with bioreactors chromatography TFF CIP systems Exposure on DCS control system would be preferable Scale up scale down processing of both upstream and downstream process Upstream processing operations seed bioreactors production bioreactors operations media and buffer preparation activities Downstream processing operations Centrifugation Microfiltration and Ultrafiltration skid systems 2 Review monitoring To ensure the preparation of the cleaning disinfectant solution and cleaning fumigation of area equipment as per the schedule and respective SOPs To ensure entire manufacturing activities to be performed as per respective SOP s guidelines To ensure that on- line entries in GMP documents like BMRs BPRs log-books etc are performed as per Valuable Documentation Practice To ensure that all documents are updated revised periodically to meet cGMP standards and as per QAD requirement Ability to mainly evaluate schedule in accordance to manufacturing processes and determine the most efficient method of accomplishing goals in order to meet the targets Supervise coach and train new and current employees i e job safety etc to meet performance expectations by providing strong leadership skill set 3 GMP compliance Validation and audit readiness To co-ordinate and support for timely completion of calibration preventive maintenance qualification validation revalidation of process units as per schedule Ensure that safety Good Manufacturing Practices GMPs and sanitation policies and procedures are met Process systems and manufacturing area readiness for GMP FDA WHO and international audits Preparation of BMR and BPR Validation protocols preparation and its execution Education Requirement Graduate or Post graduate in Science B E in biotech engineering Experience Requirement Having minimum 0-1 years experience Demonstrated ability to effectively supervise lead and build relationships at all levels within the company Skills Competencies Safety Requirements Carrying out activities related to Occupational Health Safety and Environment Management as per SOP Awareness Knowledge on the consequences of not following Standard Operating Procedures related to Occupational Health Safety and Environment Management

📌 Young Professionals (Maharashtra)
🏢 Reliance Life Science
📍 Maharashtra