Plymouth, mn: $120,488 to $192,780; other location...
Fully remote
Quality engineering
Fda regulated medical device manufacturing
Process validation maturity
Implement and provide oversight of consistent global Quality and Regulatory requirements related to elements supporting the overall operations and process controls
Job Summary
Implement and provide oversight of consistent global Quality and Regulatory requirements related to elements supporting the overall operations and process controls.
Serve as best practice/quality resource within your own discipline or as technical expert on functional or cross-functional teams/projects, acting on a global scale across all Philips businesses and factories.
We believe that we are better together than a part; for our Office-based teams, this means working in-person at least 3 days per week.
Matching Summary
Implement and provide oversight of consistent global Quality and Regulatory requirements related to elements supporting the overall operations and process controls.
Salary
Plymouth, MN: $120,488 to $192,780; Other Locations: $114,750 to $183,600 or $128,520 to $205,632; Bonus/Equity: Annual incentive bonus, sales commission or long-term incentives may be offered; Benefits: Comprehensive Philips Total Rewards benefits program
Skills & Requirements
Must-have
Quality Engineering
FDA regulated medical device manufacturing
process validation maturity
non-conformance reduction
Quality Assurance activities
Nice-to-have
creative problem-solving techniques
relentless focus on Product Quality
ability to influence change
data-driven decisions
relationship management skills
Key Requirements
Minimum of 7+ years' experience
Bachelor’s Degree in Quality, Engineering or related field
Lean Six Sigma Black Belt or Master Black Belt certified