Design Quality Engineer – Medical Devices

Philips; Bedford (MA); On-site; USD 103,000 - 163,000; Full time

Benefits offered by this job

Generous PTO

401k (up to 7% match)

HSA with company contribution

Stock purchase plan

Education reimbursement

Job summary

Philips is seeking a Design Quality Engineer in Bedford, MA. This role focuses on ensuring design quality for medical products, including risk management and complaint investigations. Candidates must have at least 3 years of experience in FDA regulated environments and a Bachelor’s Degree in a relevant field.

This position offers a salary range from $103,000 to $163,000, depending on experience. Philips also provides competitive benefits, including PTO and a 401k match.

Qualifications

• 3+ years of experience in FDA regulated medical device environments.
• Proven experience in Risk Management (ISO 14971).
• Experience in utilizing Post Market Surveillance data analytics.

Responsibilities

• Ensure appropriate quality plans are followed.
• Provide input to design processes and product realization.
• Perform routine risk management updates.

Skills

FDA regulated medical device experience

Risk Management expertise

Design Verification/Validation

Root Cause analysis

Post Market Surveillance

Education

Bachelor's Degree in Quality, Engineering or similar disciplines

Job description

Philips is seeking a Design Quality Engineer in Bedford, MA. This role focuses on ensuring design quality for medical products, including risk management and complaint investigations. Candidates must have at least 3 years of experience in FDA regulated environments and a Bachelor’s Degree in a relevant field.

This position offers a salary range from $103,000 to $163,000, depending on experience. Philips also provides competitive benefits, including PTO and a 401k match.