Work Flexibility: OnsiteSenior Manufacturing EngineerContract: Permanent + full suite of benefitsLocation: Model Farm Road, CorkBusiness Area: On-Site PositionAbout StrykerWe are excited to be named one of the by Fortune Magazine
We are proud to offer you our comprehensive rewards package, which includes bonuses, healthcare, insurance benefits, retirement programs, wellness initiatives, and service recognition programs.Position Overview:In this role, you will play a key part in developing, optimising 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.
You will be responsible for driving process efficiency and continuous improvement across all stages of complex assembly operations, ensuring validated manufacturing systems consistently deliver exceptional product quality and operational excellence.Key Responsibilities: Own and sustain manufacturing processes within value streams for Neurovascular products, ensuring product quality, process stability, and regulatory compliance.
Lead root cause analysis and implement corrective to address product and process issues.Identify and deliver continuous improvement (CI) and cost reduction projects focused on OEE, yield, and scrap reduction, applying Lean, Six Sigma, and statistical techniques.Execute process and equipment changes under Stryker's quality system, including documentation, risk assessment, validation, and change control.Support ongoing process validation (IQ/OQ/PQ) and maintain a validated state through periodic reviews and revalidations as required.Partner with Production, Quality, Maintenance, and Supply Chain teams to improve equipment uptime, throughput, and reliability.Lead data collection, analysis, and reporting on key performance metrics (yield, downtime, cost per unit, etc.) and drive improvements based on findings.Support and lead audits, CAPA closure, and documentation updates to ensure compliance with ISO ***** and FDA QSR standards.Train and mentor technicians and operators on process changes, standard work, and best practices to foster a culture of continuous improvement.Contribute to cross-site collaboration, sharing best practices and lessons learned across Stryker's Cork and global manufacturing network.Qualifications, Knowledge & SkillsBachelor's degree (or equivalent) in Manufacturing, Mechanical, Industrial, or Biomedical Engineering (or related discipline).
Minimum 2+ years of experience in manufacturing or process engineering, ideally in a regulated medical device or high-volume precision assembly environment.Proven expertise in continuous improvement, process optimisation, and problem solving (Lean/Six Sigma Green Belt preferred).
Strong understanding of manufacturing documentation, change control, and validation processes.Solid experience with CAPA management, risk analysis (PFMEA), and troubleshooting production issues.Excellent interpersonal and communication skills with the ability to influence and work cross-functionally.Strong technical judgment and a hands-on approach to resolving complex engineering challenges.Why Join Stryker CorkBe 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 that invests in its people and values integrity, accountability, and inclusion.Thrive in a culture that celebrates teamwork, continuous improvement, and life-changing innovation.
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