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Stryker

Manufactures orthopedic and surgical medical devices

Staff Quality Engineer - Quality Assurance

Quality EngineeringConfirmed live in the last 24 hours
Full-timeCarrigtohill, Carrigtwohill, Co. Cork, Ireland€54k - €90k /yr

About the Job

Requirements

  • An Honours Bachelor’s degree in Science or Engineering is required.
  • At least 4 years of experience in a Quality or Regulatory Affairs role is required; prior industry experience is desirable.
  • Proficiency in medical-device manufacturing processes, ISO 13485, and Good Manufacturing Practice (GMP) is required.
  • Lean Six Sigma training is an advantage.
  • A detailed understanding of engineering and quality principles, including risk management, Corrective and Preventive Action (CAPA), audits, and statistics, is required.
  • High-level knowledge or experience with risk-based and statistical techniques, particularly process risk, statistical sampling plans, process capability, and Gauge Repeatability and Reproducibility (R&R), is required.
  • High-level personal-computer skills and proficiency with Microsoft Word, Microsoft Excel, and PowerPoint are required.
  • Experience interacting with regulatory agencies such as the FDA, Ministry of Health, and TÜV is desired.
  • Strong knowledge of quality concepts, including risk management, CAPA, audits, and statistics, is required.
  • The candidate must demonstrate leadership and mentoring behaviors and be able to coach and guide others on technical, regulatory, and company requirements.
  • Problem-solving, analytical, and communication skills, attention to detail, and the ability to resolve conflicts constructively are required.
  • The candidate must be fluent in written and spoken English at B2 level, including writing documents and meeting minutes, participating in conference calls, technical writing, and presenting.
  • The candidate must be able to manage multiple tasks in a fast-paced environment and work as part of a multi-site team.
  • Some travel is required.

Responsibilities

  • Provide quality leadership and direction in quality assurance, quality control, and preventive activities within operations and other business functions, focusing on preventive measures and continuous improvement of products and processes.
  • Lead initiatives and projects that enhance quality performance within the business.
  • Support internal customers on quality issues and provide technical support for quality-system assessment and performance evaluation activities.
  • Coach and provide technical direction across multiple areas of expertise, and ensure compliance with regulations and standards.
  • Work with Operations and business functions to oversee and direct quality performance of products and processes.
  • Collaborate with internal and external teams to resolve quality issues.
  • Manage internal and supplier-driven non-conformances, ensuring timely investigation and closure.
  • Own and coach others in Corrective and Preventive Actions through root-cause analysis to closure.
  • Disposition non-conforming products through the Material Review Board and issue non-conformances as appropriate.
  • Coach the quality team and other business functions on quality topics and activities.
  • Lead quality initiatives and projects at local and global levels.
  • Serve as a recognized process owner and provide expertise across problem solving, risk, concession and change management, lean, Six Sigma, CAPA, statistics, validation, inspection processes, and sampling.
  • Contribute expert input to local, global, and corporate processes and represent the function on review and discussion boards and teams.
  • Provide input, assessment, and justification during concession and change-management decisions and quality issues; review and approve these matters.
  • Interpret key performance indicator trends and take action to drive continuous improvement.
  • Apply Human Error Prevention principles in the manufacturing environment.
  • Use risk-management practices and tools, demonstrate expertise in process risk, and help develop risk management by identifying opportunities and weaknesses.
  • Provide technical direction in optimizing inspection methods and sampling.
  • Participate in and potentially lead internal and external audits with regulatory representatives, present the area of expertise and business overview, and provide audit-management, logistics, and preparation oversight or deputy support as required.
  • Assist in developing validation strategies and hold validation certifications to approval level.
  • Support or lead manufacturing transfers to other plants or facilities.
  • Initiate, manage, and support shipment and product holds and potential product escapes.
  • Provide support and facilitation during internal and external audits.
  • Manage supplier relationships, including communications, performance monitoring, management of internal and external non-conformities, and timely delivery of quality materials and services.

Desired Qualifications

  • Prior industry experience.
  • Experience interacting with regulatory agencies such as the FDA, Ministry of Health, and TÜV.
  • Lean Six Sigma training.

About the Company

Stryker

Manufactures orthopedic and surgical medical devices

Stryker makes medical devices for hospitals, surgical centers and emergency responders, spanning joint implants, surgical instruments and patient transport equipment. Its Mako platform assists surgeons with joint replacement, while its neurotechnology products support brain and spine procedures and stroke treatment. Clinicians use its equipment during surgery and emergency care, and the company earns money by selling implants, disposable products and capital equipment through direct sales teams and distributors. The business also supplies training and technical support for healthcare providers using its devices. Stryker was founded in 1941 and is headquartered in Portage, Michigan.

Company size
10,001+
Company stage
IPO
Headquarters
Portage, MI
Founded
1941

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