Operator 1

• To conduct manufacturing and supportive operations to manufacturing in compliance with cGMP standards and the Quality Management System.
• To record experimental and manufacturing data and processing details in laboratory notebooks and manufacturing records to the required standard.
• Prepare, setup and clean experimental and manufacturing equipment.
• Assist with the cleaning and maintenance of the GMP and development facilities.
• Comply with assigned SOP's.
• Complete batch records and cGMP documentation in line with expected standards.
• Batch Sampling Activities
• Perform all work in a responsible and safe manner in accordance with Health and Safety policies and ensure that all Health and Safety considerations are appropriately documented prior to commencement of work.
• Maintain personnel training record at all times and proactively identify any training requirements for the job role.

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