Michael Page
Senior Quality Engineer
A global leader in advanced engineering, prototyping, and micro-manufacturing for the medical device industry, known for producing complex subcomponents like glucose monitoring wires and cardiovascular filter membranes. They operate a full-scale production facility with a collaborative, supportive culture, serving top-tier medical device companies and driving innovation through laser machining and precision manufacturing. Job Description
Senior Quality Engineer: Lead cross-functional teams to ensure robust quality systems and defect-free production. Maintain compliance with ISO 13485 and 21 CFR 820 regulations. Manage CAPAs, non-conformances, and supplier quality activities. Execute process validations, DOE, FMEA, and Gage R&R. Serve as customer liaison for quality-related issues. Support audits and act as SME during inspections. Drive continuous improvement using Lean and Six Sigma methodologies. MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants. The Successful Applicant
Senior Quality Engineer: 5+ years of quality engineering experience in medical device manufacturing. Strong knowledge of ISO 13485, 21 CFR 820, Lean, and Six Sigma. Proficient in Minitab, statistical analysis, and process validation. Skilled in CAPA, non-conformance management, and supplier quality oversight. Excellent technical writing, communication, and project management abilities. Hands-on, detail-oriented, and adaptable to fast-paced production environments. Collaborative team player with a proactive, problem-solving mindset. What's on Offer
Competitive base salary range of $80K-$100K with potential flexibility based on experience. Annual profit-sharing bonus of 3-4% of salary. Comprehensive benefits package with strong coverage. Supportive, well-performing team culture with approachable leadership. Opportunities to work on diverse, high-impact medical device projects. Regular team-building activities, including monthly lunches, seasonal events, and holiday celebrations. Strong connection with corporate leadership and room for professional growth.
A global leader in advanced engineering, prototyping, and micro-manufacturing for the medical device industry, known for producing complex subcomponents like glucose monitoring wires and cardiovascular filter membranes. They operate a full-scale production facility with a collaborative, supportive culture, serving top-tier medical device companies and driving innovation through laser machining and precision manufacturing. Job Description
Senior Quality Engineer: Lead cross-functional teams to ensure robust quality systems and defect-free production. Maintain compliance with ISO 13485 and 21 CFR 820 regulations. Manage CAPAs, non-conformances, and supplier quality activities. Execute process validations, DOE, FMEA, and Gage R&R. Serve as customer liaison for quality-related issues. Support audits and act as SME during inspections. Drive continuous improvement using Lean and Six Sigma methodologies. MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants. The Successful Applicant
Senior Quality Engineer: 5+ years of quality engineering experience in medical device manufacturing. Strong knowledge of ISO 13485, 21 CFR 820, Lean, and Six Sigma. Proficient in Minitab, statistical analysis, and process validation. Skilled in CAPA, non-conformance management, and supplier quality oversight. Excellent technical writing, communication, and project management abilities. Hands-on, detail-oriented, and adaptable to fast-paced production environments. Collaborative team player with a proactive, problem-solving mindset. What's on Offer
Competitive base salary range of $80K-$100K with potential flexibility based on experience. Annual profit-sharing bonus of 3-4% of salary. Comprehensive benefits package with strong coverage. Supportive, well-performing team culture with approachable leadership. Opportunities to work on diverse, high-impact medical device projects. Regular team-building activities, including monthly lunches, seasonal events, and holiday celebrations. Strong connection with corporate leadership and room for professional growth.