Michael Page
Senior Quality Systems Engineer - Med Device - Boxford, MA
Michael Page, Andover, Massachusetts, us, 05544
Play a key role in strengthening and evolving core quality systems
Your expertise will help shape scalable, efficient processes.
About Our Client
This company is driving innovation in advanced medical technologies that support critical care and improve patient outcomes. It offers a fast-paced, mission-driven environment where your work directly contributes to transformative healthcare solutions.
Job Description
Lead the Corrective and Preventive Action (CAPA) program, ensuring timely and effective resolution of quality issues. Manage internal audits and support external inspections to maintain compliance with regulatory standards. Monitor and report on key quality metrics, driving data-informed improvements. Collaborate cross-functionally to enhance quality system processes and documentation. Support continuous improvement initiatives across the organization's quality management system. 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.
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
Strong experience managing CAPA programs and driving root cause investigations. Solid understanding of quality system regulations and standards (e.g., ISO 13485, FDA QSR). Proven ability to lead internal audits and support regulatory inspections. Excellent analytical, organizational, and communication skills. Experience in a regulated medical or life sciences environment preferred. What's on Offer
Competitive salary and bonus. Comprehensive benefits package to support your well-being. Opportunities for professional growth and development within the engineering and manufacturing department. A collaborative work environment within the life science industry.
If you are ready to take your career to the next level, apply now to join a team dedicated to quality and innovation!
Contact
Taylor Rankin
Quote job ref
JN-072025-6786900
This company is driving innovation in advanced medical technologies that support critical care and improve patient outcomes. It offers a fast-paced, mission-driven environment where your work directly contributes to transformative healthcare solutions.
Job Description
Lead the Corrective and Preventive Action (CAPA) program, ensuring timely and effective resolution of quality issues. Manage internal audits and support external inspections to maintain compliance with regulatory standards. Monitor and report on key quality metrics, driving data-informed improvements. Collaborate cross-functionally to enhance quality system processes and documentation. Support continuous improvement initiatives across the organization's quality management system. 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.
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
Strong experience managing CAPA programs and driving root cause investigations. Solid understanding of quality system regulations and standards (e.g., ISO 13485, FDA QSR). Proven ability to lead internal audits and support regulatory inspections. Excellent analytical, organizational, and communication skills. Experience in a regulated medical or life sciences environment preferred. What's on Offer
Competitive salary and bonus. Comprehensive benefits package to support your well-being. Opportunities for professional growth and development within the engineering and manufacturing department. A collaborative work environment within the life science industry.
If you are ready to take your career to the next level, apply now to join a team dedicated to quality and innovation!
Contact
Taylor Rankin
Quote job ref
JN-072025-6786900