Stability Analyst at Cell Marque Corporation

St. Louis, Missouri, United States -

Full Time

Start Date

Immediate

Expiry Date

14 Feb, 26

Salary

43.0

Posted On

16 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Laboratory Experience, Quality Experience, Communication Skills, Interpersonal Skills, Collaboration Skills, Detail-Oriented, Organized, Project Management, Problem-Solving Skills, Analytical Skills

Industry

Biotechnology Research

Description

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 a highly motivated and detail-oriented Stability Studies Specialist to join our team. The Stability Specialist will be responsible for developing, executing and analyzing stability studies for IVD products. This role will ensure compliance to regulatory guidelines, such as IVDR. Develop and implement stability protocols according to guidelines and internal SOPs. Execute testing for stability samples, ensuring accuracy and precision. Monitor and maintain stability chambers and associated equipment. Document all data accurately in electronic systems. Analyze stability data and generate reports. Interpret stability data to assess product shelf life and storage conditions. Identify and investigate stability trends and deviations. Prepare stability reports for regulatory submissions and internal documentation. Ensure stability studies are conducted in compliance with regulatory guidelines, such as IVDR, ISO 13485. Who You Are: Minimum Qualifications: Associate Degree in Life Science (Biology, Chemistry, Biochemistry, etc.) OR High School Diploma or GED 2+ years of laboratory experience Preferred Qualifications: 2+ years quality experience Good 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 RSREMD Pay Range for this position: $24.00-$43.00 per hour. 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. 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! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Responsibilities

The Stability Analyst will develop, execute, and analyze stability studies for IVD products, ensuring compliance with regulatory guidelines. Responsibilities include monitoring stability chambers, documenting data, analyzing stability data, and preparing reports for regulatory submissions.