The successful candidate will work as a member of a team with responsibility for the introduction of products into Zimmer Biomet’s Galway facility. The initial 12-month contract will involve the setting up of finishing, cleaning and packaging processes but may include front end processes such as machining or 3d printing. Working closely with the other team members, the candidate will ensure that the processes are set-up in accordance with the governing quality system policies.
Principal Duties & Responsibilities
•Assist with the development of finishing and cleaning strategies
•Develop manufacturing instructions/operating procedures
•Development of inspection plans
•Develop PFMEA’s
•Assist in the development of routers/BOM’s
•Generate validation documentation
•Execution validations
•Work with local manufacturing and planning to ensure that all activities are captured within the local planning process
•Development of capacity plans, understand constraints, develop capital plans where appropriate
This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADA
• Level 8 Degree in Engineering or Science discipline, preferably Mechanical or Materials although other disciplines will be considered
• Previous experience in manufacture of medical devices, ideally within orthopedic joint replacement products would be a distinct advantage
• Previous experience in validations
• Good analytical and problem-solving skills
