Executive - IPQA EM
Key Responsibilities: Conduct routine environmental monitoring and assessments in various locations Collect, analyze, and interpret environmental data using specialized equipment and software Maintain
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Key Responsibilities: Conduct routine environmental monitoring and assessments in various locations Collect, analyze, and interpret environmental data using specialized equipment and software Maintain
Key Responsibilities: Conduct routine environmental monitoring and assessments in various locations Collect, analyze, and interpret environmental data using specialized equipment and software Maintain
Key Responsibilities: Water sampling and analysis Microbial Limit Test Sterility test Bioburden test Preservative efficacy test Bacterial endotoxin test. Qualification: M.Sc. (Microbiology) Experience
Key Responsibilities: Water sampling and analysis Microbial Limit Test Sterility test Bioburden test Preservative efficacy test Bacterial endotoxin test. Qualification: M.Sc (Microbiology) Experience:
Key Responsibilities: Conduct routine environmental monitoring and assessments in various locations Collect, analyze, and interpret environmental data using specialized equipment and software Maintain
Description: Responsible for ensuring the accuracy and reliability of laboratory instruments through regular calibration and preventive maintenance. This role involves the daily verification of key in
• Responsible for preparation, review, revision, control and implementation of standard operating procedures of sterile manufacturing department & warehouse department. • Responsible for preparation &
Key Responsibilities: Having a Knowledge of Instrument operation like HPLC, GC, UV, IR, Karl Fischer, Auto Titrator Good knowledge of LIMS and Documentation having Experience of working with 21 CFR co
Key Responsibilities: Conduct routine environmental monitoring and assessments in various locations Collect, analyze, and interpret environmental data using specialized equipment and software Maintain
Key Responsibilities: Environment monitoring Aseptic area behaviour and monitoring Handling of Instrument i.e NVPC and MAS. Personnel monitoring Trend analysis and reporting Sample handling Qualificat
Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitor
Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitor
Description: To ensure compliance with cGMP and regulatory requirements by performing in-process quality assurance activities on the manufacturing and packaging shop floor, including real-time monitor
Key Responsibilities: Having a Knowledge of Instrument operation like HPLC, GC, UV, IR, Karl Fischer, Auto Titrator Good knowledge of LIMS and Documentation having Experience of working with 21 CFR co
Description: This role ensures GMP and GxP compliance in dispensing, manufacturing, and packaging. Responsibilities include machine and area clearance, product sampling, in-process checks, batch recor
Key Responsibilities: Performing key activities of Supply Chain function To understand resource and capacity required to fulfill current and future demand Capacity Planning based on manufacturing capa
Key Responsibilities: Responsible to attend the training as per schedule and to ensure the training and work as per TNI. Responsible to perform and monitoring all the activities related to Aseptic are
Key Responsibilities: Performing key activities of Supply Chain function Preparing Manufacturing Plan Coordinating for RM/PM delivery with SSSM (Purchase) team Coordinating for RM/PM release with QC t
Key Responsibilities: Experience of Analyst in physical activity like handling of UV visible spectrophotometer, Karl Fischer, Water content determination, Particle Size determination, Titration. and h
Key Responsibilities: Responsible for review of URS, DQ and vendor/ supplier's documents related to qualification. Responsible for preparation and review of Validation/ Qualification protocol and repo
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