Lead Design Quality Engineer for Embedded Medical Devices

3 weeks ago


Denver, Colorado, United States Joulé Full time
Join Joulé as a Lead Design Quality Engineer for Embedded Medical DevicesAbout the Role

We are seeking a seasoned Lead Design Quality Engineer with expertise in embedded software coding, design control, and method validation to drive the development of innovative medical devices.

In this role, you will collaborate with cross-functional teams to ensure product design meets regulatory standards and customer needs, and lead efforts in agile development environments.

Key Responsibilities
  • Collaborate with I&D teams to bring medical devices to market
  • Evaluate Design and Development deliverables to ensure high-quality products meet customer needs
  • Support SW development improvements in agile environments while complying with medical device regulations
  • Anticipate roadblocks and provide direction for navigating the quality system
  • Ensure thorough root cause analysis for design changes or validation failures
  • Translate critical design attributes to design outputs
  • Guide major programs and may take on project leadership roles
  • Act as the prime technical contact, coordinating with external teams on significant matters
  • Develop technical specifications and ensure regulatory compliance (FDA)
  • Direct phases of complex engineering work, developing new approaches to problems
  • Create new processes impacting multiple disciplines
  • Contribute to business objectives, goals, budgets, and costs
  • Present complex technical information and respond to inquiries
  • Mentor junior engineers and provide cross-functional guidance
  • Consult on broad technical and industry issues
  • Work on complex issues requiring deep analysis and judgment
  • Oversee technicians and junior engineers
Requirements
  • 8 years of experience, including 3-4 in medical devices (quality for design and development in R&D or quality)
  • Bachelor of Science degree or Master of Science degree in Engineering or computer science preferred
  • Strong in design quality for embedded medical device software or software development for devices
  • Understanding of software functionality
  • Experienced in risk management and product development as a development or design quality engineer
  • Hands-on with test method validations; product knowledge required beyond document review
  • Familiar with software development and agile methodologies
  • Knowledge of 21 CFR 820.30, ISO 13485, ISO 14971, and ISO 62304
  • Skilled in technical innovation and leadership in mechanical/chemical engineering, fluids engineering, and cellular biology
We Offer
  • Competitive total reward offerings that consist of compensation, benefits, recognition, along with a wealth of other well-being, work-life and recognition programs
  • Multiple group medical, dental and vision plans
  • A robust wellness program
  • Life insurance and disability coverages
  • Voluntary programs such as group accident, hospital indemnity, critical illness, pet insurance and much more
  • A 401(k) plan with a matching contribution
  • Vacation and sick time programs for associates


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