Michael Page
Senior Quality Manager - Medical - Danvers, MA
Michael Page, Danvers, Massachusetts, us, 01923
Drive innovation & elevate outcomes across healthcare specialties
Your expertise directly influences product excellence and operational success.
About Our Client
My client, located on the North Shore of Massachusetts is a global medical technology company develops and supplies advanced tools, biotech solutions, and lab support for clinical professionals. Its mission is to simplify complex procedures and improve outcomes across a range of health care specialties through innovation and collaboration.
Job Description
Lead the development, implementation, and continuous improvement of quality systems and processes across product development and manufacturing operations. Ensure compliance with global regulatory standards and internal quality requirements, including oversight of audits, CAPAs, and risk management activities. Collaborate cross-functionally to support design control, process validation, and design transfer, ensuring quality integration throughout the product life cycle. Monitor production processes using data-driven methodologies to identify trends, deviations, and opportunities for improvement. Oversee supplier quality programs, including qualification, audits, and incoming material inspections to ensure consistent product standards. Drive strategic quality initiatives, mentor team members, and foster a culture of accountability, innovation, and operational excellence. Support regulatory inspections and customer audits, ensuring readiness and effective communication of quality system performance. Utilize project management tools to balance competing priorities and deliver high-impact quality outcomes. 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
Bachelor's degree in engineering, life sciences, or a related technical field; advanced degree preferred. 8+ years of experience in quality assurance or quality engineering within a regulated industry, ideally medical technology or life sciences. Proven leadership experience managing quality teams and driving cross-functional collaboration. Deep understanding of quality systems, regulatory standards (e.g., ISO 13485, FDA 21 CFR Part 820), and risk management practices. Strong background in design control, process validation, and product life cycle management. Experience with supplier quality management, audits, CAPA, and continuous improvement methodologies. Excellent analytical, communication, and project management skills, with the ability to influence and lead across functions. Comfortable working in a fast-paced, evolving environment with a focus on operational excellence and innovation. What's on Offer
Competitive salary and bonus potential. Opportunity to work within a growing company in the life science industry. Comprehensive benefits package and potential for career advancement. Collaborative work environment focused on innovation and excellence.
Take the next step in your career as a Senior Manager of Quality by applying today!
Contact
Taylor Rankin
Quote job ref
JN-102025-6864541
My client, located on the North Shore of Massachusetts is a global medical technology company develops and supplies advanced tools, biotech solutions, and lab support for clinical professionals. Its mission is to simplify complex procedures and improve outcomes across a range of health care specialties through innovation and collaboration.
Job Description
Lead the development, implementation, and continuous improvement of quality systems and processes across product development and manufacturing operations. Ensure compliance with global regulatory standards and internal quality requirements, including oversight of audits, CAPAs, and risk management activities. Collaborate cross-functionally to support design control, process validation, and design transfer, ensuring quality integration throughout the product life cycle. Monitor production processes using data-driven methodologies to identify trends, deviations, and opportunities for improvement. Oversee supplier quality programs, including qualification, audits, and incoming material inspections to ensure consistent product standards. Drive strategic quality initiatives, mentor team members, and foster a culture of accountability, innovation, and operational excellence. Support regulatory inspections and customer audits, ensuring readiness and effective communication of quality system performance. Utilize project management tools to balance competing priorities and deliver high-impact quality outcomes. 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
Bachelor's degree in engineering, life sciences, or a related technical field; advanced degree preferred. 8+ years of experience in quality assurance or quality engineering within a regulated industry, ideally medical technology or life sciences. Proven leadership experience managing quality teams and driving cross-functional collaboration. Deep understanding of quality systems, regulatory standards (e.g., ISO 13485, FDA 21 CFR Part 820), and risk management practices. Strong background in design control, process validation, and product life cycle management. Experience with supplier quality management, audits, CAPA, and continuous improvement methodologies. Excellent analytical, communication, and project management skills, with the ability to influence and lead across functions. Comfortable working in a fast-paced, evolving environment with a focus on operational excellence and innovation. What's on Offer
Competitive salary and bonus potential. Opportunity to work within a growing company in the life science industry. Comprehensive benefits package and potential for career advancement. Collaborative work environment focused on innovation and excellence.
Take the next step in your career as a Senior Manager of Quality by applying today!
Contact
Taylor Rankin
Quote job ref
JN-102025-6864541