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.
Your Role:
In the Analytical Scientist role, you’ll be working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma in St. Louis, MO, and will serve as an individual contributor in the Process and Analytical Development organization. You will be working in a lab setting on analytical method development and optimization for external customers in the field of Antibody Drug Conjugates (ADC). The role will include problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing and quality control organizations.
Responsibilities:
Perform hands-on work executing analytical methods Qualify and transfer analytical methods into Quality Control to support GMP release testing Document and communicate experimental results with strong customer-facing skills Promptly deliver data, adhering to ALCOA+ principles for proper data documentation, and make data-driven decisionsIndependent management of daily activities, lead project initiatives and lead process improvement initiativesAct as a mentor to less experienced scientists, evolving into an emerging subject matter authority capable of troubleshooting issues as they emerge
Who You Are:
Minimum Qualifications:
Bachelor’s Degree in Chemistry, Biochemistry, Engineering, or other Scientific discipline with 3+ years of experience in method development within a GMP/pre-GMP environmentOR
Master’s Degree in Chemistry, Biochemistry, Engineering, or other Scientific discipline with 1+ years of experience in method development within a GMP/pre-GMP environmentOR
PhD in Chemistry, Biochemistry, Engineering, or other Scientific discipline
Preferred Qualifications:
Hands-on experience in separation science, notably the theory, operation, data interpretation and troubleshooting of UPLC, RP-HPLC, SEC, HIC and/or IEX Experience with protein analytics and spectroscopy (UV and slope)Prior experience working with customers and matrix teamsWorking knowledge of Microsoft Office suite and digital documentation (modern data acquisition systems and electronic notebooks)
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