Info
St. Louis (MO)
St. Louis (MO), USA
Merck
Merck
Full-time
Full-time
Quality Control (QC), Analytical chemist
Quality Control (QC), Analytical chemist
$66,800 - $110,300 / annually
$66,800 - $110,300 / annually

Stability Specialist

Inactive
Merck - Career

Our passion for science and technology is what drives our more than 64,000 employees across 66 countries to find solutions to some of today’s toughest challenges and create more sustainable ways to live.

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.

Stability Specialist

Your Role

MilliporeSigma is seeking a highly motivated and detail-oriented Stability Specialist to join our team. The Stability Specialist will be responsible for developing, executing and analyzing stability studies for IVD (In Vitro Diagnostic products). This role will ensure compliance to regulatory guidelines, such as ISO13485 and IVDR. Responsibilities include:

  • 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:

  • Bachelor's Degree in Biology, Chemistry, Biochemistry or other Life Science discipline
  • 2+ years of laboratory or Quality experience

Preferred Qualifications:

  • Previous experience with IHC testing
  • Previous experience writing stability protocols and reports
  • 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 - $66,800 - $110,300 / annually

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!

 

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