Senior Process Development Engineer - Trauma & Extremities Division
Hybrid role, 3 days on site in Cork
What you will do:
* Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures.
* Ensure quality of process and product as defined in the appropriate operation and material specifications.
* Assist in the selection of components and equipment based on analysis of specifications, reliability and regulatory requirements.
* Support capital acquisition activities.
* Analyze equipment to establish operating data, conduct experimental tests and result analysis. Participate in process review meetings.
* Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches.
* Complete capability studies for in-process inspection and generate subsequent Inspection documentation.
* Conduct MSA studies for new products and new processes.
* Provide training for manufacturing team members.
* Ensure adherence to GMP and safety procedures.
* All other duties as assigned.
Required Qualifications:
B.S in Mechanical Engineering or related engineering discipline
Self-starter with demonstrated efficient work methods, analytical & problem-solving skills, and ability to handle multiple tasks.
Preferred Experience:
* Strong communication skills with the ability to effectively work cross-functionally and externally as required.
* Basic knowledge of manufacturing processes, materials, product, and process design.
* Ability to read and interpret complex engineering drawings and understand geometrical dimensioning and tolerancing.
* Experience in an FDA regulated or regulated industry beneficial but not essential as training is provided.
* High level of PC skills required.
* Excellent attention to detail.
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