Quality Systems Engineer

Philips

Bedford, MA, US
$102,480 to $163,968; not specified; generous pto,...
Fully remote
Qms compliance
Capa processes
Document control
The Quality Systems Engineer is responsible for ensuring an efficient/compliant Quality Management System (QMS), including analysis, development and revision of QMS processes, performance monitoring and continuous improvement, ensuring accuracy and compliance with relevant standards

Job Summary

  • The Quality Systems Engineer is responsible for ensuring an efficient/compliant Quality Management System (QMS), including analysis, development and revision of QMS processes, performance monitoring and continuous improvement, ensuring accuracy and compliance with relevant standards.
  • We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve.
  • The pay range for this position in Bedford, MA is $102,480 to $163,968. 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 Quality Systems Engineer is responsible for ensuring an efficient/compliant Quality Management System (QMS), including analysis, development and revision of QMS processes, performance monitoring and continuous improvement, ensuring accuracy and compliance with relevant standards.

Salary

$102,480 to $163,968; Not specified; Generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement

Skills & Requirements

Must-have

  • QMS compliance
  • CAPA processes
  • Document Control
  • Audits
  • Training management

Nice-to-have

  • Innovative approaches
  • Cross-functional leadership
  • Mentoring less experienced engineers

Key Requirements

  • Minimum 5+ years experience in FDA regulated (ISO 13485) medical device quality operations/manufacturing
  • Bachelor’s Degree in Quality, Engineering or similar disciplines
  • Experience managing/maintaining training metrics/matrix
  • Proven experience leading cross-functional teams
  • Detailed experience/knowledge in CAPA processes
  • Experienced in Data analysis, understanding QMS metrics/KPIs
  • US work authorization

Work Rights

US work authorization required

Tailored Resume

Cover Letter