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Stryker

Manufactures orthopedic and surgical medical devices

Senior Engineer, Advanced Quality

Quality EngineeringPosted on Nov 9
Full-timePortage, MI, USA$77.7k - $129.5k /yr

About the Job

Requirements

  • A bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, Science, or a related discipline is required.
  • At least 2 years of full-time work experience in Quality Engineering, Technical Engineering, Product Development, or a related engineering role within a research and development or manufacturing environment is required.
  • Experience applying quality engineering methods within product development or manufacturing processes is required.

Responsibilities

  • Lead quality engineering activities for new product development, ensuring compliance with FDA Quality System requirements, ISO 13485, and internal quality standards.
  • Lead product risk management activities, including risk analysis, failure mode evaluation, risk mitigation, and assessment of product reliability.
  • Apply quality engineering tools and statistical methods to evaluate components, assemblies, processes, and finished products throughout design and development.
  • Lead human factors engineering and design validation activities to verify products meet defined user needs, intended uses, and safety requirements.
  • Develop reliability testing strategies, including accelerated test methods and correlation of test results with expected field performance.
  • Support design verification, process validation, manufacturing process development, and inspection methods for components and finished products.
  • Partner with Research & Development, Manufacturing, Product Engineering, and other cross-functional teams to review technical deliverables and resolve quality issues throughout development.
  • Support nonconformance and corrective and preventive action investigations using structured problem-solving, root cause analysis, and appropriate corrective action methods.

Desired Qualifications

  • At least 1 year of experience in Advanced Quality Engineering, Design Quality Engineering, or a related new product development quality role.
  • Experience working within a regulated medical device or other regulated manufacturing environment.
  • Experience applying ISO 13485, Good Manufacturing Practice, and Good Documentation Practice requirements.
  • American Society for Quality Certified Quality Engineer (CQE), Certified Reliability Engineer (CRE), Certified Six Sigma Black Belt (CSSBB), or equivalent training or experience.
  • Training or certification in Geometric Dimensioning and Tolerancing (GD&T).

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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