Quality Engineer - Medical Device - Hudson, NH

• Join a culture that values continuous learning & professional development
• Work with products that play a vital role in improving lives & advancing tech

About Our Client
My client is a medical device manufacturer specializing, supporting a variety of surgical fields (e.g., vascular, neurosurgery, robotic). They design, produce, and sell these highquality devices directly from their southern NH facility, with over 30 years in operation serving surgical teams nationally and globally.
Job Description

• Establish and uphold quality management systems to ensure compliance with industry standards and customer requirements.
• Perform regular audits to assess compliance with quality standards and identify areas for improvement.
• Collect and interpret data to monitor product quality and implement corrective actions as necessary.
• Work closely with manufacturing, engineering, and other departments to address quality issues and implement process improvements.
• Investigate quality problems, determine root causes, and develop effective solutions to prevent recurrence.
• Ensure that products and processes meet applicable regulatory and customer-specific requirements.
• Educate team members on quality standards, procedures, and best practices to promote a culture of quality.
• Maintain accurate records of quality activities, including inspection results, audit findings, and corrective actions.
• Identify opportunities for process enhancements and contribute to ongoing quality improvement projects.

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

• A bachelor's degree in engineering.
• 2-5 years of experience in a lean manufacturing environment, preferably within the medical device sector.
• Ability to identify issues, analyze root causes, and implement corrective actions.
• Strong analytical skills with a focus on quality assurance and continuous improvement.
• Experience in managing and maintaining quality documentation, ensuring compliance with industry standards.
• Proven ability to collaborate with suppliers to ensure product quality and adherence to specifications.
• Familiarity with the Production Part Approval Process (PPAP), including preparation and submission of required documentation.

What's on Offer

• Competitve benefits
• Engage in cutting-edge projects that push the boundaries of material science and engineering.
• Benefit from a culture that values continuous learning and professional development.
• Job stability

Contact
Taylor Rankin
Quote job ref
JN-062025-6774482