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: 

 

At MilliporeSigma, the Associate Quality Scientist will perform Quality Control activities in support of raw materials of cGMP products at our Cherokee site, including routine testing, in-house and compendial.  In addition, testing of Environmental Monitoring (EM) and cleaning verification samples will be performed.

 

Perform routine testing of raw material samples through adherence to applicable GMP requirements.Utilize written procedures to perform routine and non-routine product testing.Revise procedures through use of the Document Management System (DMS) following Good Documentation Practices (GDP).Work in accordance with current GMPs and demonstrate proper laboratory safety and housekeeping practices.Participate in method development and validation activities to support product testing.Contribute to support function of the laboratory through participation in laboratory audits to maintain compliance.Participate in deviation investigations.Contribute to process improvement projects.Wear personal protective equipment including but not limited to:  safety glasses, gloves and respirator.

 

Who You Are:

 

Minimum Qualifications:

 

Bachelor's Degree in Chemistry, Chemical Engineering, or other Life Sciences discipline1+ years of GMP laboratory experience

 

Preferred Qualifications:

 

Knowledge of general laboratory techniques, both theoretical and practicalWorking Knowledge of GMP for pharmaceutical manufacturing, including 21 CFR 210, 211, and ICH Q7AProficient in Microsoft Word, Excel, and AccessExcellent time management and organizational skillsAbility 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