Due to taking on an exciting new project, an opportunity has arisen for a Process Engineer to join the operations team. Within this role you would be responsible for stabilising and improving the manufacturing processes for all company products. An initial part of the role will involve working within the specific project team in the preparation of process, materials and validation.
Key Tasks and Responsibilities: Ensure project is clearly characterized/mapped at all stages, Key Performance Indicators are understood and critical control/inspection points are identified. Write and execute PQ validation. Carry out all process FMEAs and Risk Analysis' Define and generate Bill of Materials and Control Plan. A device master record. Component assembly, and finished product specifications. Assembly drawings controlled. Manufacturing and assembly procedures Component incoming inspection procedures. Manufacturing in-process inspection and test procedures. Support IQ and PQ documentation. Finished product test and inspection procedures. Labelling and packaging specifications and procedures, acceptance criteria. Product shipping procedures documented.
The Candidate: The individual will have a strong knowledge of medical device production process requirements and be capable of problem solving. Will be Degree (BEng/BSc/BA) or eqiuvlent plus relevant experience as a Process Engineer in medical manufacturing environment or similar. An ability to communicate effectively to a wide audience and accept and follow up the views and opinions of others.
An award winning, manufacturing company based in Central Scotland.
For more information or to apply for this position please contact Richie at firstname.lastname@example.org or call 01506 517215
Job Reference: RW/15519
Closing Date: 27-Jun-2012