Associate Quality Scientist

MilliporeSigma; St. Louis (MO); On-site; USD 55,000 - 75,000; Full time

Job summary

Join a leading company as an Associate Quality Scientist, where you will support Quality Control activities for cGMP products. This role involves routine testing, method development, and ensuring compliance with GMP standards. Ideal candidates have a Bachelor’s degree in a relevant field and at least one year of laboratory experience, along with strong organizational skills and teamwork abilities.

Qualifications

• At least 1 year of GMP laboratory experience.
• Knowledge of laboratory techniques, both theoretical and practical.

Responsibilities

• Perform routine testing of raw material samples following GMP requirements.
• Engage in deviation investigations and contribute to process improvement projects.

Skills

Time Management

Team Collaboration

Education

Bachelor's Degree in Chemistry

Bachelor's Degree in Chemical Engineering

Bachelor's Degree in Life Sciences

Tools

Microsoft Word

Microsoft Excel

Microsoft Access

Job description

Join to apply for the Associate Quality Scientist role at MilliporeSigma

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 diverse community of people, customers, patients, and the planet. We are always seeking curious minds who 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 supporting raw materials for cGMP products at our Cherokee site, including routine testing (in-house and compendial), Environmental Monitoring (EM), and cleaning verification samples.

• Perform routine testing of raw material samples following GMP requirements.
• Use written procedures for routine and non-routine product testing.
• Revise procedures via the Document Management System (DMS) following Good Documentation Practices (GDP).
• Operate in accordance with current GMPs, maintaining proper laboratory safety and housekeeping.
• Participate in method development and validation activities.
• Support laboratory functions through participation in audits to ensure compliance.
• Engage in deviation investigations.
• Contribute to process improvement projects.
• Wear personal protective equipment, including safety glasses, gloves, and respirators.

Who You Are

Minimum Qualifications:

• Bachelor's Degree in Chemistry, Chemical Engineering, or related Life Sciences discipline.
• At least 1 year of GMP laboratory experience.

Preferred Qualifications:

• Knowledge of laboratory techniques, both theoretical and practical.
• Familiarity with GMP for pharmaceutical manufacturing, including 21 CFR 210, 211, and ICH Q7A.
• Proficiency in Microsoft Word, Excel, and Access.
• Strong time management and organizational skills.
• Effective team collaboration skills.

What We Offer

We value diverse backgrounds, perspectives, and experiences, believing they drive innovation and excellence. We are committed to creating an inclusive environment where everyone can develop and grow. Join us in building a culture of inclusion that empowers everyone to work their magic and champion human progress!

Apply now and be part of a team dedicated to Sparking Discovery and Elevating Humanity!