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Limerick, LK, V94, IE
Job details
Work flexiblity: Hybrid
Req ID: R530767
Employee type: Full Time
Job category: Engineering
Travel: 20%
Relocation: No
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Job description
Senior/Staff Engineer, Process Development, Advanced Operations
(Permanent Position) (Hybrid Working - Limerick/Cork)
What you will do
- Executes assigned project elements with an emphasis on manufacturing systems and procedures required for the manufacture of new products.
- 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 that all activities are completed and documented in accordance with the Stryker new product development procedures.
- Lead manufacturing and inspection conversations with both Product Development and Suppliers.
- Own multiple product families from early design concepts to launch, while maintaining Project Manager's timeline.
- Participate in PFMEA, Control Plan, SOP and PPAP generation associated with product transfers and launches.
- Conduct MSA studies for new products and new processes.
- Will 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.
What you will need:
Required:
- Bachelor’s Degree (Hons) Level 8 in an Engineering Discipline
- Senior – 2 plus years work experience
- Staff – 4 plus years work experience
- Self-starter with demonstrated efficient work methods, analytical & problem-solving skills and ability to handle multiple tasks in a fast paced environment.
- Must be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing.
- Ability to plan, organise and implement concurrent tasks.
- Ability to express ideas and collaborate effectively with multidisciplinary teams,
Preferred:
- Experience within the medical device/manufacturing industry.
- Experience in an FDA regulated or regulated industry beneficial.
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