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Job Requirements of Senior Quality Manager:
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Employment Type:
Full-Time
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Education:
4 Year Degree
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Location:
Littleton, MA (Onsite)
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Senior Quality Manager
This role provides strategic leadership over site‑wide quality systems, driving a culture of quality excellence while ensuring products meet stringent customer and regulatory requirements. It oversees quality assurance, quality control, and supplier quality teams, leading audits, continuous‑improvement initiatives, and cross‑functional alignment to achieve reliable, compliant, and 'right‑first‑time' performance.
Client Details
This organization is a global provider of advanced fluid‑management technologies used in highly regulated industries such as pharma, biotech, and manufacturing. It develops engineered solutions ranging from filling and dispensing systems to fully automated production equipment, all designed for precision, sterility, and reliability. The company operates internationally and supports customers with a strong focus on innovation, technical expertise, and high‑quality engineering.
Description
- Develop and implement quality management systems and processes in line with industry standards.
- Lead quality assurance and control activities to ensure compliance with regulatory requirements.
- Identify areas for process improvement and drive initiatives to enhance operational efficiency.
- Collaborate with cross-functional teams to ensure quality objectives are met across all projects.
- Manage audits and inspections, ensuring all quality documentation is accurate and up to date.
- Provide training and guidance to team members on quality standards and best practices.
- Monitor quality metrics and generate reports for senior management.
- Stay updated on industry trends and advancements to drive innovation in quality management.
Profile
A successful Senior Quality Manager should have:
- Bachelor's degree in Engineering or a scientific discipline
- Proven experience as a Site Quality Manager with end-to-end quality ownership
- 5-10 years of people management experience
- Medical Device background required with strong knowledge of ISO 13485
- Certificates by accredited bodies in Leading Auditing, Quality Management, process improvement methodologies
- Experience with regulatory compliance and conducting audits.
- Excellent leadership and team collaboration skills.
- A results-oriented mindset with a focus on continuous improvement.
Job Offer
- Competitive salary range of $165,000 - $180,000 USD annually.
- Comprehensive benefits package to support your well-being.
- Opportunities for career growth within a respected medium-sized organization.
- Collaborative and innovative work environment.
- Chance to make a significant impact on quality standards.
If you are passionate about quality management and ready to take on an influential role in the Engineering & Manufacturing sector, we encourage you to apply today!
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.