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Stryker

Manufactures orthopedic and surgical medical devices

Senior Design Quality Engineer - Software/Electrical

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timePortage, MI, USA$77.7k - $129.5k /yr

About the Job

Requirements

  • A bachelor's degree in Software Engineering, Electrical Engineering, Computer Science Engineering, or a related engineering discipline.
  • At least 2 years of experience in quality, manufacturing, new product development, software, electrical engineering, or a related engineering field.

Responsibilities

  • Partner with R&D to ensure software and electrical product designs meet quality requirements for safety, effectiveness, reliability, manufacturability, cybersecurity, and usability; support collection of customer and market feedback to inform design requirements and validate the design through production launch.
  • Lead risk management activities for new product development teams by developing risk management plans and reports, conducting risk reviews, and verifying implementation and effectiveness of design and process risk controls.
  • Partner with Product Security and R&D to implement cybersecurity best practices and address security-related risks and requirements in product design.
  • Participate in design reviews and track how software and electrical design features, specifications, documentation, test methods, and manufacturing processes mitigate risks throughout development.
  • Lead design validation activities, including human factors usability engineering.
  • Support design verification planning and execution and contribute to final design verification and validation reports.
  • Support product design and quality transfers to internal or external manufacturing facilities.
  • Analyze and define critical quality attributes for products and processes through risk analysis techniques.
  • Partner with Operations and suppliers to implement robust process controls for electrical components, assemblies, software-enabled systems, and manufacturing processes.
  • Support PPAP planning by defining and communicating applicable PPAP requirements to component suppliers and supporting PPAP approval.

Desired Qualifications

  • Experience within the medical device or manufacturing industry.
  • Familiarity with ISO 13485 medical device quality management systems and ISO 14971 medical device risk management.
  • Experience supporting software and/or electrical product development, design controls, verification, validation, or cybersecurity activities.
  • Experience with data analysis, statistical analysis, sampling plans, statistical process control, or Minitab.
  • Applied knowledge of advanced quality tools such as FMEA, root cause analysis, and mistake proofing/Poka-Yoke.
  • Ability to read and interpret electrical schematics, technical specifications, test requirements, and engineering documentation.
  • Six Sigma certification.
  • ASQ certification or a master's degree in engineering.

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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