Senior Manufacturing Engineer
Contract: Permanent + full suite of benefits
Location: Model Farm Road, Cork
Business Area: Neurovascular
Position Overview
In this role, you will play a key part in developing, optimizing, and sustaining manufacturing processes for advanced neurovascular medical devices used in the treatment of strokes and aneurysms. The position demands a strong emphasis on precision, process reliability, and adherence to stringent regulatory and quality standards.
Key Responsibilities
Apply a prioritized approach in Value Centred Engineering to achieve key opportunities in quality, service and cost.
Assist in the development of a world‑class manufacturing group proficient in process improvement and problem‑solving using Six‑Sigma tools.
Provide technical leadership on all product and process issues.
Monitor line performance and execute structured event plans to remediate systemic issues.
Develop and implement appropriate supporting documentation, SOPs and process work instructions compliant with Good Manufacturing Practices (GMP).
Lead technical improvements under the Continuous Improvement Program (CIP) and transfer processes from development or other facilities.
Provide guidance for Process/Maintenance Technicians and other Manufacturing/Equipment Engineers.
Support new product and process introduction, ensuring all activities are completed and documented per Stryker's New Product Development Process.
Conduct process validation (VP, IQ, OQ, PQ) and associated documentation.
Perform Gauge R‑R studies for products and new processes.
Carry out structured problem solving and facilitate cross‑functional projects (value stream and cross‑functional).
Interface with cross‑functional team members and 3rd‑party vendors to support day‑to‑day operations and achieve business targets.
Support continuous improvement initiatives aligned with Quality Policy, Quality System, and regulatory requirements.
Monitor and report on variables affecting business performance metrics, proactively identifying and resolving issues.
Enforce Environmental Health and Safety (EHS) requirements on site.
Manage material risks on the production floor in cooperation with Supplier Quality engineers.
Serve as a subject‑matter expert for regulatory audit purposes.
Provide out‑of‑hours support as required by management or shutdowns and equipment failures.
Qualifications, Knowledge & Skills
Level 8 Degree in Mechanical Engineering or equivalent technical experience.
2‑4+ years of experience in a manufacturing environment.
Proven project management skills through delivery of business‑critical projects.
Technical leadership, influencing and providing direction to engineers, technicians and operators.
Demonstrable analytical and problem‑solving skills, process improvement orientation, and ability to handle multiple tasks in a fast‑paced environment.
Strong decision‑making ability and negotiation skills.
Experience with FDA‑regulated or similar industry and Six‑Sigma and Lean Manufacturing concepts.
Green or Black Belt Six‑Sigma qualification.
Why Join Stryker Cork
Be part of a world‑class Neurovascular manufacturing hub focused on precision, safety, and innovation.
Collaborate with a talented, diverse team committed to operational excellence.
Grow your career in a globally recognised organisation investing in its people.
Thrive in a culture that celebrates teamwork, continuous improvement and life‑changing innovation.
EEO Statement
Stryker Corporation is an equal‑opportunity employer. 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.
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