Senior Quality Engineer - Medical Device - Canton, MA

Michael Page; Canton (MA); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Comprehensive benefits

Job summary

Michael Page is seeking a Senior Quality Engineer to support and continuously improve a robust Quality Management System in a medical device manufacturing environment in Canton, MA. You will lead quality initiatives, perform risk management, and drive continuous improvement across cross‑functional teams.

Responsibilities include CAPA, MRB, FMEA, MSA, Gage R&R, supplier quality, audits, and verification activities. A strong background in ISO 13485 and data‑driven decision making is required.

Qualifications

• Bachelor's degree in Engineering, Quality, Manufacturing, or a related technical discipline.
• 5-10 years of quality engineering experience in medical device or regulated manufacturing.
• Strong understanding of ISO 13485 QMS and regulatory compliance.
• Experience with CAPA, nonconforming materials, calibration systems, and root cause analysis methodologies.

Responsibilities

• Support the effectiveness, maintenance, and continuous improvement of the Quality Management System (QMS).
• Partner with leadership and cross-functional teams to ensure ISO 13485 compliance.
• Mentor and train Quality Engineers and support onboarding and development.
• Provide shop floor quality support, troubleshoot manufacturing issues, and lead root cause investigations.
• Own Risk Management activities, including FMEA and risk mitigation.

Skills

Quality engineering

ISO 13485

CAPA

Root cause analysis

Minitab

Data analysis

GD&T

MSA

Metrology

RCA

Education

Bachelor's degree in Engineering/Quality/Manufacturing

Tools

Minitab

ERP systems

Microsoft Office

Job description

We are seeking a Senior Quality Engineer to support and continuously improve a robust Quality Management System while ensuring compliance with ISO 13485 standards. This role combines hands-on manufacturing support, process improvement leadership, customer quality ownership, and cross-functional collaboration to drive operational excellence.

Our client is a highly respected advanced manufacturing organization serving innovative and rapidly evolving regulated industries. The company invests heavily in quality, technology, and continuous improvement, creating an environment where engineers can make a meaningful impact on products that matter.

Description

• Support the effectiveness, maintenance, and continuous improvement of the Quality Management System (QMS).
• Partner with leadership and cross-functional teams to ensure compliance with ISO 13485 requirements.
• Mentor and train Quality Engineers while supporting onboarding and professional development initiatives.
• Provide shop floor quality support, troubleshoot manufacturing issues, and lead root cause investigations.
• Own Risk Management activities, including FMEA development and ongoing risk mitigation efforts.
• Manage customer complaints, returns, and corrective action activities to ensure timely resolution.
• Support equipment qualification and validation activities including IQ, OQ, and PQ protocols.
• Execute Measurement System Analysis (MSA) and Gage R&R studies to improve inspection reliability.
• Identify, implement, and validate new inspection technologies and quality control methods.
• Lead quality improvement projects through statistical analysis and data-driven decision-making.
• Manage engineering change processes and associated risk assessments.
• Support supplier quality activities, including Approved Supplier List evaluations and performance reviews.
• Develop and maintain quality documentation, SOPs, work instructions, and forms.
• Perform product inspections and other quality-related activities as require

Profile

• Bachelor's degree in Engineering, Quality, Manufacturing, or a related technical discipline.
• 5-10 years of quality engineering experience within medical device or medical component manufacturing.
• Strong understanding of ISO 13485 Quality Management Systems and regulatory compliance.
• Experience with CAPA, nonconforming materials, calibration systems, and root cause analysis methodologies.
• Proficiency with metrology equipment, inspection systems, and measurement techniques.
• Ability to interpret engineering drawings, blueprints, and GD&T specifications.
• Experience supporting customer, FDA, or third-party quality audits is highly desirable.
• Strong data analysis skills with statistical software such as Minitab.
• Proficiency with Microsoft Office applications and ERP systems.

Job Offer

• Opportunity to lead quality initiatives in a medical device manufacturing environment.
• Significant influence on operational performance, compliance, and continuous improvement efforts.
• Exposure to advanced manufacturing processes and cutting-edge technologies.
• Collaborative culture with direct interaction across engineering, operations, and leadership teams.
• Strong potential for professional growth, leadership development, and long-term career advancement.

We are seeking a Senior Quality Engineer to support and continuously improve a robust Quality Management System while ensuring compliance with ISO 13485 standards. This role combines hands-on manufacturing support, process improvement leadership, customer quality ownership, and cross-functional collaboration to drive operational excellence.

Client Details

Our client is a highly respected advanced manufacturing organization serving innovative and rapidly evolving regulated industries. The company invests heavily in quality, technology, and continuous improvement, creating an environment where engineers can make a meaningful impact on products that matter.

Description

• Support the effectiveness, maintenance, and continuous improvement of the Quality Management System (QMS).
• Partner with leadership and cross-functional teams to ensure compliance with ISO 13485 requirements.
• Mentor and train Quality Engineers while supporting onboarding and professional development initiatives.
• Provide shop floor quality support, troubleshoot manufacturing issues, and lead root cause investigations.
• Own Risk Management activities, including FMEA development and ongoing risk mitigation efforts.
• Manage customer complaints, returns, and corrective action activities to ensure timely resolution.
• Support equipment qualification and validation activities including IQ, OQ, and PQ protocols.
• Execute Measurement System Analysis (MSA) and Gage R&R studies to improve inspection reliability.
• Identify, implement, and validate new inspection technologies and quality control methods.
• Lead quality improvement projects through statistical analysis and data-driven decision-making.
• Manage engineering change processes and associated risk assessments.
• Support supplier quality activities, including Approved Supplier List evaluations and performance reviews.
• Develop and maintain quality documentation, SOPs, work instructions, and forms.
• Perform product inspections and other quality-related activities as require

Profile

• Bachelor's degree in Engineering, Quality, Manufacturing, or a related technical discipline.
• 5-10 years of quality engineering experience within medical device or medical component manufacturing.
• Strong understanding of ISO 13485 Quality Management Systems and regulatory compliance.
• Experience with CAPA, nonconforming materials, calibration systems, and root cause analysis methodologies.
• Proficiency with metrology equipment, inspection systems, and measurement techniques.
• Ability to interpret engineering drawings, blueprints, and GD&T specifications.
• Experience supporting customer, FDA, or third-party quality audits is highly desirable.
• Strong data analysis skills with statistical software such as Minitab.
• Proficiency with Microsoft Office applications and ERP systems.

Job Offer

• Opportunity to lead quality initiatives in a medical device manufacturing environment.
• Significant influence on operational performance, compliance, and continuous improvement efforts.
• Exposure to advanced manufacturing processes and cutting-edge technologies.
• Collaborative culture with direct interaction across engineering, operations, and leadership teams.
• Strong potential for professional growth, leadership development, and long-term career advancement.
• Comprehensive benefits package.
  

Desired Skills and Experience

• 5-10 years of Quality Engineering experience in medical device or regulated manufacturing environments.
• Strong knowledge of ISO 13485, QMS management, CAPA, and compliance requirements.
• Experience with FMEA, risk management, root cause analysis, and corrective actions.
• Hands-on validation expertise including IQ, OQ, PQ, MSA, and Gage R&R studies.
• Ability to interpret engineering drawings, blueprints, and GD&T specifications.
• Proficient with Minitab, quality audits, metrology equipment, and statistical analysis tools

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.