Execute defined procedures to manufacture high potency ADC/ API's product in support of launched products and clinical trial programmed to GMP standards. Working effectively in an organized manner in order to adhere to the planned schedule Contribute effectively to a team working environment but also have the ability and confidence to work on an individual basis within the production team. Accurately recording information required for batch records Updating and reviewing plant documentation, from PI Sheets to SOP'S. Maintain high ESH Standards, carrying out all work in accordance with appropriate EHS systems. Have a working knowledge of risk management systems and procedures enabling escalation of deviation as appropriate. * Demonstrate flexibility, self-control, and interpersonal awareness within the team environment.
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