Quality Engineer - Weekend Shift

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.  

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. 

Your Role: 
As a Quality Engineer in our Danvers, MA, production site, you play a key role in the success of the Quality and Manufacturing organizations.

Weekend Shift: Friday - Sunday 6am - 6pm

Key responsibilities include but are not limited to:

• Utilize root cause analysis tools to complete product and process related investigations.
• Lead and support risk assessments utilizing FMEA.
• Review and improve standard operating procedures and other production documentation.
• Support customer-facing improvement projects that incorporate evolving customer and industry requirements.
• Conduct internal GMP and ISO audits.
• Support deviation resolution in production and corrective action implementation.
• Assures products are manufactured in compliance with regulatory requirements and manufacturing plans are monitored for compliance to ISO, GMP, and MilliporeSigma standards.
• Monitor and trend process performance and drive continuous improvement.
• Lead projects with cross functional teams to improve in-process quality, reduce customer complaints, and increase production efficiency.

Who You Are:

Minimum Qualifications:

• Bachelors Degree in Chemical Engineering, Biology, or other Engineering or Life Science Discipline.

Preferred Qualifications:

• 1+ years of experience in Biotechnology, Pharmaceutical, Medical Device, or Life Science industries.
• Lean Six Sigma and/or root cause analysis training.
• Experience leading risk assessments using tools such as FMEA.
• Experience with Quality Systems. (e.g. Deviation, CAPA, Change Control, Documentation Management)
• Experience conducting internal/customer/supplier audits.
• Demonstrated ability to write and execute test protocols and reports.
• CQA or CQE. 
• Demonstrate strong quality knowledge: GMP/GDP, ISO standards. 
• Ability to adapt and thrive in a constantly changing business environment.
• Experience with Microsoft Office Suite.

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