Quality Engineer - Engineered Materials - Durham, NH

The Quality Engineer role offers an opportunity to play a pivotal part in ensuring product excellence and compliance within a dynamic manufacturing environment. This position involves developing and implementing quality control systems, conducting inspections and tests, and collaborating with cross-functional teams to drive continuous improvement and maintain high-quality standards.

Client Details

My client is an innovative manufacturing company specializes in transforming high-performance material into custom-engineered components for critical applications in industries like medical devices, aerospace, and biotechnology. With a strong focus on precision, cleanroom assembly, and rapid prototyping, they offer a dynamic environment where technical creativity and problem-solving are at the forefront of delivering cutting-edge solutions

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.

Profile

• 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.

Job 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

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.