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 has an opening as a Quality Scientist performing review at our Cherokee / St. Louis site!  This team helps support our manufacturing of custom products including active pharmaceutical ingredients, excipients, and raw materials. In this role you will be responsible for reviewing the documentation and data generated for analysis of GMP products. This review may include data supporting raw materials, in-process and/or final products. You will be responsible for verifying that documentation and raw data meet good documentation requirements, are technically acceptable, all calculations are appropriate and correct, and specifications are met.  Additional expectations may include the review of new or updated procedures for both technical soundness and allowance for appropriation documentation.  Review of audit trails, data integrity, and GDP required. Importantly, you will have primary responsibility for review of raw data, protocols and reports for all analytical method undergoing validation.  You will be critical in ensuring that validated methods support the final product specifications through review of procedural updates after validation activities are complete.

This is a Monday - Friday Day shift position 

Who You Are:

 

Minimum Qualifications:

 

Bachelor’s Degree in Chemistry, Biology, or other life science field.

 

Preferred Qualifications:

 

3+ years of GMP experience in pharmaceutical, biopharmaceutical or chemistry. Excellent attention to detail.Intermediate knowledge of Word and Excel.Technical knowledge of wet chemistry, chromatography, and electrophoretic testing.1+ years of experience with analytical method validation. Effective communication in cross-functional teams.

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