Quality Scientist at Millipore Corporation in St. Louis, Missouri

Job Description:

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:



The Quality Scientist (QC Microbiology) is responsible for microbiology related analysis including but not limited to in-process, drug substance, raw material and water sample endotoxin analysis; method validation, development and associated endotoxin verification of in-process and drug substance samples. Job duties include:

• Ensuring that suitable written records and work undertaken are kept in accordance with cGMP and company procedures.


• Working within various internal departments to improve and execute processes used in an ICHQ7 environment.


• Assisting with OOS/OOT investigations and root cause analysis investigations.


• Interacting with the production and laboratory personnel regularly to ensure adequate communication and feedback for quality-related services to internal customers.


• Maintaining and updating relevant Ops.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.



Who you are:




Minimum Qualifications:

• Bachelor's Degree in Biology, Chemistry, or other life science discipline.


• 5+ years of QC lab experience in endotoxin and bioburden analysis (chromogenic, turbidimetric and gel-clot methods).

Preferred Qualifications:

• Current API knowledge and/or experience.


• Knowledge of SOPs, cGMPs, GLP, GDP and quality control processes.


• Knowledge and understanding of endotoxin testing, LER/hold time studies; verification testing.


• Experience with ICH Q7, 21CFR210, USP < 85>, USP < 1085> and EP pharmacopeia requirements.


• Experience writing technical documents and reports.


• Strong knowledge of aseptic technique and practices.


• Ability to perform minor troubleshooting on microbiological processes and associated laboratory equipment.


• Experience with documentation control: writes, reviews, and approves operating procedures, reports, protocols, and other QC controlled documents.


• Experience independently writing verification protocols and final reports.


• Familiar with basic scientific/regulatory principles.


• Excellent written and verbal communication skills.


• Capacity to work independently.


• Fosters collaboration and teamwork.


• Ability to simultaneously manage multiple tasks/priorities good computer skills, including proficiency in MS Word, MS Excel, MS PowerPoint, and the ability to learn and operate other specific application software.


• Good problem-solving and time management 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 Apply Now