Quality Control Scientist 2nd shift

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 Scientist, Quality Control Reviewer 2nd Shift role includes the following key accountabilities:

• Analyze complex and unique issues, applying scientific rationale for root cause analysis and implementing corrective actions.
• Perform analytical and peer review of cGMP data to ensure accuracy and quality, adhering to ALCOA+ principles.
• Prioritize in-process control testing review and communicate effectively to minimize manufacturing downtime.
• Train newer laboratory staff and assist with review of in-process and release testing.
• Maintain a safe, audit-ready, and clean laboratory by managing supplies and performing general housekeeping.
• Investigate deviations, identify root causes, and author complex investigations with communication to internal and external customers.
• Review various reports, including product changeover and method transfer summaries, and manage projects and timelines.
• Ensure compliance with regulatory requirements (ICH Q7, 21 CFR Parts 11, 210, 211) and agency guidelines (FDA, OSHA, EPA, DNR, DOT).
• Will work a 2nd shift schedule of 1300 to 2330 Monday-Thursday and travel between Madison and Verona sites as required.

Physical Attributes:

• Work in analytical testing lab with hazardous and toxic chemicals.

Who You Are 

Minimum Qualifications:

• Bachelor’s Degree in Chemistry, Biology, or other Life Science discipline
• 5+ years experience in a GMP or GLP setting.

Preferred Qualifications:

• Understanding of 21 CFR Part 11, 210 and 211, and ICH Q7.
• Excellent written and verbal communication skills, as well as good documentation practices and attention to detail.
• Knowledge and understanding of analytical chemistry techniques.
• Proficient in LCMSMS analysis.
• Adequate technical writing skills to author reports, training memos and operating procedures.

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!