Stryker SENIOR ENGINEER, PROJECTS, ADVANCED OPERATIONS in Limerick, Ireland

Requisition ID 24309BR

Job Title SENIOR ENGINEER, PROJECTS, ADVANCED OPERATIONS

Group Orthopaedics

Division Joint Replacement

Business Function Research and Development

Country IRELAND

City Limerick

Employment Category Full Time

Percent Travel Required Up to 20%

Shift 1st

About Stryker

Stryker is one of the world’s leading medical technology companies and together with our customers, we are driven to make healthcare better. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. Stryker products and services are available in over 100 countries. All qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Job Description / Information

  • 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.

  • 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.

  • May lead/support capital acquisition activity from specifying equipment, contract negotiation, Installation and validation.

  • Will analyse equipment to establish operating data, conduct experimental test 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.

Minimum Qualifications

  • B.S in Mechanical Engineering or related engineering discipline with 4 or more years’ experience or a related masters degree.

  • Proven track record of working in a team based environment.

  • Innovative thinker - should be able to envisage new and better ways of doing things.

Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams. Be open minded with the ability to recognise good ideas.

Experience in executing complex problem solving techniques related to manufacturing/design technical issues. Good instincts and sound judgement for mechanical and structural design.

  • Good understanding of Design for Manufacturing (DFM), related statistical tools and validation/verification techniques.

  • Excellent 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 have the ability to understand geometrical dimensioning and tolerancing.

  • Certified in validation activities.

  • Experience in an FDA regulated or regulated industry beneficial.

  • High level of PC Skills required.

  • Excellent attention to detail.

All qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status.

Stryker is an EO employer – M/F/Veteran/Disability