Associate Quality Scientist

The businesses of Merck KGaA, Darmstadt, Germany; 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'll perform Quality Control activities in a GMP environment. Utilize your Chemistry or Life Sciences background to ensure compliance and contribute to product testing and process improvements. This role offers the chance to work in a collaborative team dedicated to innovation in science and technology.

Qualifications

• 1+ years of GMP laboratory experience.
• Knowledge of general laboratory techniques.

Responsibilities

• Perform routine testing of raw material samples adhering to GMP requirements.
• Participate in method development and validation activities.

Skills

Collaboration

Time Management

Organizational Skills

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

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 samplesthrough adherence to applicable GMP requirements.
• Utilizewritten 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 discipline
• 1+ 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

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!