What are the responsibilities and job description for the Stability Supervisor position at MilliporeSigma?
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 Stability Studies Supervisor to oversee day to day activities related to stability studies and lead the team of associated coordinators and scientists, ensuring compliance with regulatory requirements and internal protocols. This role involves managing the stability program, coordinating study design and execution, and analyzing stability data.
- Lead and mentor a team of stability coordinators and scientists, 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.
- Ensure proper storage and handling of stability samples in controlled environmental chambers.
- Oversee the execution of analytical testing for stability samples, ensuring accuracy and precision.
- Review and approve stability data, ensuring compliance with established specifications.
- Review stability study protocols and reports.
- Guarantee accurate and up-to-date stability records and documentation.
- Ensure compliance with regulatory guidelines, such as IVDR, ISO 13485.
- Collaborate with other departments to support product development and regulatory submissions.
- 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 (Chemistry, Biology, etc.) or Engineering (Chemical Engineering, Mechanical Engineering, etc.)
- 3 years of experience in a quality leadership role
Preferred Qualifications:
- Strong communication, interpersonal, and collaboration skills
- Ability to work effectively in a cross-functional team environment
- Detail-oriented, organized, and able to manage multiple projects simultaneously
- Problem-solving and analytical skills
- Experience with eQMS systems
- Strong understanding of IVD regulations, guidance documents, and related standards (e.g., ISO 13485, MDSAP, IVDR)
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
