Manufacturing Technician - Night Shift

Overview

Work Your Magic with us! Start your next chapter and join Millipore Sigma. 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.

The Manufacturing Technician 4 – Night Shift at our St. Louis Cherokee site is a key role within our GMP Manufacturing. Expectations is to ensure “Compliance” and “Readiness” within our GMP Operations teams, enabling high manufacturing success. Standard operations involve facility preparations, on-the-floor formulations, automated/manual ultrafiltration, and chromatography.

• Support manufacturing operations 24/7, 12 hour shifts, 6:00pm – 6:30am, including a shift differential.
• Evaluate products according to established protocols and perform operations in support of the group and department.
• Safely perform operations to meet quality expectations and dispose cleaning and process waste per approved procedures.
• Maintain required training to perform tasks/assignments.
• Perform routine processes and unit operations such as buffer formulation, ultrafiltration, and chromatography.
• Clean equipment and working areas during and after operations.
• Support facility functions (e.g., maintain equipment, prepare reagents, restock supplies, waste disposal).
• Communicate the status of operations and convey concerns to the supervisor.
• Provide complete and accurate records consistent with quality guidelines, utilizing quality approved operating procedures and documenting activities with adherence to GDP standards.
• Ensure all applicable logbooks are completed as required by current procedures.
• Interact with other departments as needed and perform procedures independently and as part of a team.
• Improve processes through application of experience and principles, in compliance with change control.
• Develop and assist in the implementation of process improvement, safety, quality, and 6S.
• Take action to resolve unsafe conditions.

• Stand for extended periods of time.
• Lift, push, and pull up to 50 lbs.
• Wear mask, safety shoes, gloves, Tyvek suits, respirator, and related personal protective equipment.

• High school diploma or GED.
• 6+ months of experience working in a cGMP environment.

• cGMP experience.
• Prior experience in an API manufacturing environment.
• Strong mechanical aptitude.
• Demonstrated process improvement experience.
• Familiarity with FDA, EMA, and other regulatory standards.
• Demonstrated knowledge and experience in various computer skills, including Windows (Word, Excel, PowerPoint, etc.).

Pay Range for this position: $31.00 - $47.00 per hour.

Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.

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!