<p>Work Your Magic with us! Start your next chapter and join MilliporeSigma.</p> <p>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.</p> <p>This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.</p> <p>Your Role</p> <p>The Quality Engineer in Danvers, MA, is crucial to the success of both the Quality and Manufacturing teams at our production site. Key responsibilities of the role include, but are not limited to:</p> <ul> <li>Utilize root cause analysis tools to complete product and process related investigations </li><li>Lead and support risk assessments utilizing FMEA </li><li>Review and improve standard operating procedures and other production documentation </li><li>Support customer-facing improvement projects that incorporate evolving customer and industry requirements </li><li>Conduct internal GMP and ISO audits </li><li>Support deviation resolution in production and corrective action implementation </li><li>Assure products are manufactured in compliance with regulatory requirements and manufacturing plans are monitored for compliance to ISO, GMP, and MilliporeSigma standards </li><li>Monitor and trend process performance and drive continuous improvement </li><li>Lead projects with cross functional teams to improve in-process quality, reduce customer complaints, and increase production efficiency </li></ul> <p>Who You Are</p> <p>Minimum qualifications:</p> <ul> <li>Bachelor's Degree in Mechanical Engineering, Chemical Engineering, or other Engineering discipline OR in Biology, Chemistry, or other Life Science discipline </li></ul> <p>Preferred Qualifications:</p> <ul> <li>1+ year of experience in Biotechnology, Pharmaceutical, Medical Device, or Life Science industries </li><li>Lean Six Sigma and/or root cause analysis training </li><li>Experience leading risk assessments using tools such as FMEA </li><li>Experience with Quality Systems (e.g. Deviation, CAPA, Change Control, Documentation Management) </li><li>Experience conducting internal/customer/supplier audits </li><li>Demonstrated ability to write and execute test protocols and reports </li><li>Demonstrate strong quality knowledge: GMP/GDP, ISO standards </li></ul> <p>RSREMD</p> <p>Pay Range for this position - $67,200 - $123,100 / annually</p> <p>The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.</p> <p>What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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!</p> <p>Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!</p>