Biocon
Department DetailsRole Summary1. ENSURE PROCESS EQUIPMENT ARE QUALIFIED THROUGH COMPREHENSIVE STRATEGIES AND AT THE STATE OF QUALIFICATION AT ALL TIMES. THIS INCLUDES AND NOT LIMITED TO CLEANING VALIDATION, EQUIPTMENT VALIDATION (IQ, PQ), PROCESS VALIDATION (PQ, PV), RE QUALIFICATIONS, SAT, FAT'S.…
Department DetailsRole Summary1. Prepare equipment qualification protocol, execution of protocol and summary report 2. Prepare performance requalification protocol and execution of the protocol according to equipment requalification planner. 4. Issuance of documents. 5. Prepare initial document (e.g. SLIA and URS)…
Department DetailsRole SummaryOrganize, direct and monitor all line (secondary and tertiary packing) activities necessary for the timely production of high quality products, in a cost effective manner, under safe conditions, and according to current Good Manufacturing Practices (cGMP). Prepares daily/weekly…
Department DetailsRole SummaryLead chemical safety management program within plant Support in industrial hygiene, process safety and pest control Lead PPE management enforcement program in consultation Track to ensure all the hygiene monitoring such as LEV, Noise, CHRA and Chemical monitoring…
Department DetailsRole SummaryOrganize, direct and monitor all line (secondary and tertiary packing) activities necessary for the timely production of high quality products, in a cost effective manner, under safe conditions, and according to current Good Manufacturing Practices (cGMP). Prepares daily/weekly…
Department DetailsRole SummaryOrganize, direct and monitor all line (secondary and tertiary packing) activities necessary for the timely production of high quality products, in a cost effective manner, under safe conditions, and according to current Good Manufacturing Practices (cGMP). Prepares daily/weekly…
Department DetailsRole Summary1. To plan day to day shift activities in coordination with the superior to carry out production activity in order to achieve production targets. 2. To ensure that all production activities are carried out in compliance with the…
Department DetailsRole Summary1. To plan day to day shift activities in coordination with the superior to carry out production activity in order to achieve production targets. 2. To ensure that all production activities are carried out in compliance with the…
Department DetailsRole Summary1. Responsible for all operation and maintenance related activities inclusive of in house preventive maintenance activities to Central Utilities Facility (CUF) consists of Chiller Plant, Steam Generation Plant, WWTP as well as repair/maintenance activities of external contractors and…
Department DetailsRole Summary1 To manage the complete operations for DSP 1, DSP2 (Reaction area) 2 Production planning and control of operations to meet the business requirements in coordination with cross functional team 3 Coordination with PE/MSAT and development team for…
Department DetailsRole Summary1. Ensure adherence to cGMP requirements. 2. Ensure adherence to EHS compliance at QC Analytical Laboratory. 3. Ensure Good Documentation Practise (GDP) is in place and applied in recording of QC daily activities for easy traceability and facilitate…
Department DetailsRole Summary1 To follow the established procedures and policies of the company pertaining to EHS and ensure implementation of safety practices at work place 2 To involve in preparation HAZOP, aspect/impact register and reviewing the adequacy where ever applicable…
Department DetailsRole Summary1. Plan and execute Technology Transfer process from Biocon R&D to drug product manufacturing sites and execute Developmental, Optimization, Scale up, Exhibit, Process validation batch manufacturing. 2. Serve as a scientific and technical representative for process related aspects.…
Department DetailsRole Summary1. Plan and execute Technology Transfer process from Biocon R&D to drug product manufacturing sites and execute Developmental, Optimization, Scale up, Exhibit, Process validation batch manufacturing. 2. Serve as a scientific and technical representative for process related aspects.…
Department DetailsRole Summary1. Plan and execute Technology Transfer process from Biocon R&D to drug product manufacturing sites and execute Developmental, Optimization, Scale up, Exhibit, Process validation batch manufacturing. 2. Serve as a scientific and technical representative for process related aspects.…
Department DetailsRole Summary Get trained on the assigned SOP\'s & ensure the training completed on time for self as per the curriculum. Performing In process QA activities primarily routine in process checks, line clearance as per SOP. Online reviewing of…
Department DetailsRole Summary Get trained on the assigned SOP\'s & ensure the training completed on time for self as per the curriculum. Performing In process QA activities primarily routine in process checks, line clearance as per SOP. Online reviewing of…
Department DetailsRole Summary Get trained on the assigned SOP\'s & ensure the training completed on time for self as per the curriculum. Performing In process QA activities primarily routine in process checks, line clearance as per SOP. Online reviewing of…
Department DetailsRole Summary Get trained on the assigned SOP\'s & ensure the training completed on time for self as per the curriculum. Performing In process QA activities primarily routine in process checks, line clearance as per SOP. Online reviewing of…
Department DetailsRole Summary1. To plan day to day shift activities in coordination with the superior to carry out production activity in order to achieve production targets. 2. To ensure that all production activities are carried out in compliance with the…
Department Details Role Summary Manages the day to day operations including assisting the staff, who support Administrative computing, Networking, User services, PABX/Telecommunications Administration, Access Control Backup, and other information technology functions. Coordinate with corporate IT team and establish IT departmental…
Department Details Role Summary Identification and raising deviation, change control and compiling other cGMP related documents in coordination with QA Responsible for preparation, review, and revision of SOP, EOP and batch records. Responsible to maintain two way communication with superior…