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Quality Scientist

 

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

 

To perform Quality Control activities at our Cherokee Site in support of raw materials of cGMP products, including routine testing (in-house and compendial) and peer review of data.  In addition, testing of Environmental Monitoring (EM) and cleaning verification samples will be performed. Specific responsibilities include:

 

  • Perform routine testing of raw material samples through adherence to applicable GMP requirements. Assure adequately trained to perform tasks/assignments
  • Utilize written procedures to perform routine and non-routine product testing
  • Work in accordance with current GMPs and demonstrate proper laboratory safety and housekeeping practices
  • Contribute to support function of the laboratory through participation in laboratory audits to maintain compliance
  • Participate in deviation investigations
  • Contribute to process improvement projects

 

Who You Are

 

Minimum Qualifications:

 

 • Bachelor's Degree in Chemistry, Chemical Engineering, or other Life Sciences discipline

 • 3+ years of GMP laboratory experience

 

Preferred Qualifications:

 

  • Knowledge of general laboratory techniques, both theoretical and practical
  • Working Knowledge of GMP for pharmaceutical manufacturing, including 21 CFR 210, 211, and ICH Q7A
  • Proficient in Microsoft Word, Excel, and Access
  • Excellent time management and organizational skills
  • Ability to collaborate effectively in a team environment

 

RSREMD


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

 

Job Requisition ID:  284042
Location:  St. Louis
Career Level:  D - Professional (4-9 years)
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

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Job Segment: Laboratory, Pharmaceutical, Chemistry, Developer, Science, Technology, Quality

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