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Staff Engineer, Advanced Operations, Carrigtwohill
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Client:
Stryker European Operations Limited
Location:
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
7a2b5a7cb581
Job Views:
3
Posted:
01.07.2025
Expiry Date:
15.08.2025
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Job Description:
Work Flexibility: Hybrid or Onsite
23 month fixed term hybrid role based in Carrigtwohill, Cork
Responsible for creating a work practice and environment that pushes the boundaries of conventional manufacturing & metrology.Role success will be gauged by this individual’s contribution in coaching the engineering team to effectively meet and/or exceed new product metrics including product cost, process performance and time to market.
Responsibilities
1. Determines the technical objectives of engineering assignments and makes decisions regarding the direction and the results of the assignment.
2. Will monitor and control progress of work ensuring sound application of engineering principles and the appropriate use of policies and procedures.
3. Lead capital acquisition activity from specifying equipment, contract negotiation, Installation and validation.
4. Will analyze equipment to establish operating data, conduct experimental test and result analysis. May lead or act as independent reviewer in process review meetings.
5. Will coach and mentor others on functionally related topics.
6. Provides on-going status reports including periodic reviews progress and evaluation of results to management.
7. 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.
8. Ensure quality of process and product as defined in the appropriate operation and material specifications.
9. Will select components and equipment based on analysis of specifications, reliability and regulatory requirements. Work with quality engineers to develop component specific testing and inspection protocols.
10. Participate in PFMEA, Control Plan, SOE/MAP and PPAP generation associated with product transfers and launches.
11. Ensure adherence to GMP and safety procedures.
12. Operates with appreciable latitude for unreviewed action or decision.
13. Review and approval of validation documentation.
Qualifications/Work Experience Preferred
14. 4 or more years’ experience
15. Proven track record of working in a team based environment.
16. Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams. Be open minded with the ability to recognize good ideas.
17. Innovative thinker - should be able to envisage new and better ways of doing things.
18. Experience in executing complex problem solving techniques related to manufacturing/design technical issues. Good instincts and sound judgement for mechanical and structural design.
19. Good understanding of Design for Manufacturing (DFM), related statistical tools and validation/verification techniques.
20. Excellent analytical skills, ability to plan, organize and implement concurrent tasks.
21. Good knowledge of manufacturing processes, materials, product and process design.
22. Must be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing.
23. familiar with validation activities.
24. Experience in an FDA regulated or regulated industry beneficial.
25. Excellent attention to detail.
Travel Percentage: 10%
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