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:

MilliporeSigma is seeking an experienced Operational Quality Assurance (QA) Supervisor to oversee the quality assurance activities for our Cell Marque IVD business.  The Operational QA Supervisor monitors production processes to ensure compliance with quality standards and addresses non-conformances proactively. 

Lead and mentor a team of Quality Assurance Specialists, fostering a collaborative and high-performing work environment. Develop and manage daily work schedules, effectively assigning tasks and prioritizing workloads to optimize team efficiency and meet production timelines. Conduct regular training sessions, provide ongoing coaching, and deliver constructive performance feedback to team members, ensuring continuous skill development and adherence to quality standards. Proactively implement and enforce quality standards within operational processes, utilizing risk assessment tools such as FMEA, Fishbone diagrams, and 5-Why analysis to identify and mitigate potential quality risks.  Oversee and monitor production processes, promptly addressing quality deviations, documenting non-conformances, and implementing risk-based resolutions to maintain product integrity. Manage and provide quality assurance support for customer complaints, ensuring timely investigations, effective resolutions, and thorough documentation. Evaluate and provide quality assurance support for product and process changes, ensuring all modifications are properly documented, validated, and implemented in accordance with established procedures. Utilize statistical data and trend analysis to monitor key quality metrics, identify areas for improvement, and implement data-driven strategies to enhance overall QA performance. Actively participate in customer and regulatory audits, ensuring compliance with established standards and providing necessary documentation and support.

 

Who You Are: 

Minimum Qualifications:

Bachelor's Degree in Science (Biology, Chemistry, etc.) or Engineering (Chemical Engineering, Mechanical Engineering, etc.)3+ years of experience in a quality leadership role 

Preferred Qualifications:

Strong understanding of IVD regulations, guidance documents, and related standards (e.g., ISO 13485, MDSAP, IVDR)Strong communication, interpersonal, and collaboration skillsAbility to work effectively in a cross-functional team environmentDetail-oriented, organized, and able to manage multiple projects simultaneously. Problem-solving and analytical skillsExperience with eQMS systems 

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