Staff Manufacturing Engineer - Value Stream

Stryker Corporation; Cork; On-site; EUR 60,000 - 80,000; Full time

Job summary

A leading medical device manufacturer in Cork seeks a Staff Manufacturing Engineer to optimize and sustain processes for advanced neurovascular devices. The role emphasizes achieving regulatory compliance and driving continuous improvement using Lean and Six Sigma methodologies. Candidates should have a Bachelor's degree in a related field and at least 4 years of relevant experience. Join the team for a collaborative work environment and a focus on innovation in medical technologies.

Benefits

Comprehensive rewards package

Bonuses

Healthcare benefits

Retirement programs

Qualifications

• 4+ years of experience in manufacturing or process engineering in a regulated environment.
• Expertise in Lean/Six Sigma for process improvement.
• Strong knowledge of manufacturing documentation and validation processes.

Responsibilities

• Ensure product quality and regulatory compliance in manufacturing processes.
• Lead root cause analysis and implement corrective actions.
• Drive continuous improvement projects with Lean and Six Sigma techniques.

Skills

Continuous improvement

Problem solving

Process optimisation

Interpersonal skills

Education

Bachelor’s degree in Manufacturing, Mechanical, Industrial, or Biomedical Engineering

Job description

Work Flexibility: Hybrid**Staff Manufacturing Engineer (Value Stream)****Contract:** Permanent + full suite of benefits **Location:** Model Farm Road, Cork **Business Area:** **Work Type:** On-Site**About Stryker** We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you our comprehensive rewards package, which includes bonuses, healthcare benefits, insurance, 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 the 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 13485 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 & Skills*** Bachelor’s degree (or equivalent) in **Manufacturing, Mechanical, Industrial, or Biomedical Engineering** (or related discipline).* Minimum **4+ 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 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** that invests in its people and values integrity, accountability, and inclusion.* Thrive in a culture that celebrates teamwork, continuous improvement, and life-changing innovation.#IJTravel Percentage: 0%