Senior Design Quality Engineer

Philips

Bothell, United States
$133,560 to $213,696; not specified; comprehensive...
Fully remote
Design control process
Process validation strategies
Quality improvement projects
The Senior Design Quality Engineer is responsible for the entire design control process, from validating design inputs to overseeing verification, validation, and design transfer, as well as leading comprehensive process validation strategies to ensure new products meet quality and regulatory standards during production

Job Summary

  • The Senior Design Quality Engineer is responsible for the entire design control process, from validating design inputs to overseeing verification, validation, and design transfer, as well as leading comprehensive process validation strategies to ensure new products meet quality and regulatory standards during production.
  • Leads quality improvement projects by integrating quality, reliability, and Post Market Surveillance (PMS) insights into all stages of the product lifecycle, driving continuous enhancement of product quality and reliability.
  • Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.

Matching Summary

The Senior Design Quality Engineer is responsible for the entire design control process, from validating design inputs to overseeing verification, validation, and design transfer, as well as leading comprehensive process validation strategies to ensure new products meet quality and regulatory standards during production.

Salary

$133,560 to $213,696; Not specified; Comprehensive Philips Total Rewards benefits program

Skills & Requirements

Must-have

  • Design control process
  • Process validation strategies
  • Quality improvement projects
  • Risk management activities
  • CAPA processes
  • Continuous improvement techniques

Nice-to-have

  • Integrate quality insights
  • Build stakeholder relationships
  • Expert guidance and mentorship

Key Requirements

  • 7+ years experience in FDA regulated medical device environments
  • Minimum Bachelor’s Degree in Quality, Engineering or similar
  • US work authorization required

Work Rights

Must have US work authorization

Tailored Resume

Cover Letter