





To be a part of a highly-skilled team delivering innovative solutions to complex challenges in an automated manufacturing process. To provide support and assistance with Engineering project management and documentation in compliance with site, corporate and external regulatory requirements. Examples of this include developing machine user requirements specifications, and the development and execution of equipment qualification testing protocols to prove that the machine functions as required. Work could include devising, planning, and running trials on manufacturing equipment, collecting and analysing data and writing reports. Exposure and insight to our validation procedures for qualifying production equipment that is used for manufacturing components for medical devices.