Permanent Hybrid Role
Location: Stryker Anngrove, Carrigtwohill, Cork
Position Summary
Working as part of the Trauma & Extremities team, based in Cork, you will be executing on New Product Introductions (NPIs) alongside external suppliers and our Stryker China facilities. You will execute the innovation and development of assigned project elements with an emphasis on the manufacturing process, technology and procedures required for the manufacture of new products.
Using the latest engineering techniques to reduce product time to market whilst adhering to regulatory requirements, project deadlines and product costs.
What you will do
* Execute assigned project elements with an emphasis on manufacturing systems and procedures.
* Employ project management best practice to reduce product time to market whilst adhering to regulatory requirements, project deadlines and product costs.
* Provide engineering support for new product and process introductions, ensuring 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. Work with quality engineers to develop component‑specific testing and inspection protocols.
* Support capital acquisition activity from specifying equipment, contract negotiation, installation and validation.
* Analyze equipment to establish operating data, conduct experimental tests and result analysis. Lead and/or 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.
* Review and approval of validation documentation.
* All other duties as assigned.
What you need
* B.S. in Mechanical Engineering or related engineering discipline with up to 2 years’ experience.
* Self‑starter with demonstrated efficient work methods, analytical & problem solving skills and the ability to handle multiple tasks in a fast‑paced environment.
* Enjoy working in a fast‑paced, dynamic and results‑oriented team environment.
* Good interpersonal skills – able to express ideas and collaborate effectively with multidisciplinary teams.
* Innovative thinker – able to envisage new and better ways of doing things.
* Good analytical skills, ability to plan, organise and implement concurrent tasks.
* Good knowledge of manufacturing processes, materials, product and process design.
* Must be able to read and interpret complex engineering drawings and understand geometrical dimensioning and tolerancing.
* Experience in an FDA‑regulated or regulated industry is beneficial.
* High level of PC skills required.
* Excellent attention to detail.
If you are interested in this role, please apply in confidence.
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