Quality Engineering Supervisor

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

Your Role:

We are seeking a motivated Quality Engineering Supervisor to support device manufacturing at the Jaffrey Manufacturing site. This position will manage a small team of Quality Engineers and Quality Technicians and oversee three rapidly growing manufacturing work centers, partnering with Operations, Engineering, Product Management (Marketing) and EHS.

The Supervisor will provide guidance and mentorship to his/her expanding team of quality engineers and quality technicians. In addition to the supervisory requirements, the candidate will also be responsible for providing day-to-day Quality Engineering support for a fast-paced device manufacturing operation, including:

• Evaluation of out-of-specification conditions and providing guidance for the disposition of non-conforming product and raw materials
• Leading quality investigations (RCA and CAPA management)
• Perform statistical analysis and trending to assess and monitor product/process performance
• Working with cross functional teams to set the requirements to support product and process modifications; ensuring that Change Control requirements are met based on internal company procedures and applicable industry standards and regulations
• Lead and participate in the creation of risk assessments (product and process- FMEA)
• Participate in product validation and equipment qualifications by establishing acceptance criteria, statistical sampling plans, data analysis, and write validation protocols and reports
• Create and revise Standard Operating Procedures, Test Methods, and other documents
A Shift: Monday - Friday 8AM - 5PM

Who You Are:

Minimum Qualifications:

• Bachelors of Science Degree in a Scientific or Engineering discipline
2 years of Quality Engineering experience

Preferred Qualifications:

• Prior supervisory experience directly leading and managing a team
• ASQ CQE
• Strong communication skills with the ability to collaborate at all levels and functions of the organization
• Demonstrated ability to conduct quality investigations including root cause analysis and determining corrective / preventative actions
• Understanding or experience with ISO & FDA regulations (such as 21 CFR 820, 210 & 211)
• Pragmatic data driven risk-based decision maker with strong problem-solving ability
• Collaborative and motivated team player. Always looking to share and advance best practices
• Experience with relevant data analysis software (i.e., Minitab)

• Black Belt or Green Belt certificate
• Master’s degree
• Additional Leadership experience in an FDA regulated environment (pharmaceutical, biotechnology, or medical device)
Working knowledge of Electronic Quality Systems (CAPA, Change Control, Documentation Management)

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html