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:

Working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma in St. Louis, MO, this role will serve as an individual contributor in the Process and Analytical Development organization.  The role will involve working in a lab setting on process development and optimization for external customers in the field of Antibody Drug Conjugates (ADC) or other Antibody Conjugates.  The role will require problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing and quality control organizations. 

 Responsibilities:

Serve as a subject matter expert in process and analytical development, perform troubleshooting / providing efficient and innovative solutions, and supporting transfer to GMP manufacturingUtilize customer-facing skills, document experimental results, communicate results to all stakeholders, author method development and qualification documents, contribute to information for customer proposalsServe as a project lead and ensure project deliverables are on quality and on time, develop multiple technical approach plans as needed to solve problems and mitigate risk, ensure methods are in place for efficient GMP startIndependently lead project teams, influence exemplary work in other team members, lead process improvement initiatives, scout for new technologies / emerging trends, proactively consider the impact of quality, regulatory, manufacturing, and safety requirements when planning project activities.

 

Who You Are: 

Minimum Qualifications:

Bachelor’s Degree in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline with 6+ years of research experience         

 OR

Master’s Degree in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline with 2+ years of research experience

 OR

PhD in Chemistry, Biochemistry, Biomedical Engineering or other Scientific discipline with 1+ years of research experience

 

Preferred Qualifications:

Extensive hands-on process development experience in chromatography, ultrafiltration, and/or reaction kineticsWorking knowledge of Microsoft Office suite and digital documentation (modern data acquisition systems and electronic notebooks) as well as experience with advanced data analysis and/or statistical software systemsKnowledge of GMP and regulatory requirements as well process transfersExperience working with or leading cross-functional matrix teamsExcellent time management, written and verbal communication skills

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