Responsibilities
* 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.
#J-18808-Ljbffr