Manufacturing Technician 4 - Night 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 Manufacturing Technician 4 – Night Shift at our St. Louis Cherokee site is a key role within our GMP Manufacturing. Expectations are 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. Job duties include:

• This role will support 24/7 manufacturing operations and work 12 hour shifts from  6PM – 630 AM.
• Evaluate products according to established protocols and perform operations in support of the group and department. 
• Safely perform operations to meet quality expectations.  Safely and properly dispose cleaning and process waste per approved procedures.
• Maintain required training to perform tasks/assignments.
• Perform routine processes and unit operations. Buffer formulation, ultrafiltration, and chromatography are standard.
• Clean equipment and working areas during and after operations.
• Support functions of the facility (e.g., maintain equipment, prepare reagents, and restock supplies, waste disposal).
• Communicate the status of operations and convey concerns to the supervisor.
• Provide complete and accurate records consistent with quality guidelines.  Utilize quality approved operating procedures and document activities with adherence to GDP standards.
• Ensure all applicable logbooks are completed as required by current procedures.
• Interact with other departments as needed and performs procedures independently and 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. 

Physical Attributes:

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

Who You Are

Minimum Qualifications:

• High School Diploma or GED
• 6 + months of experience working in a cGMP environment

Preferred Qualifications:

• 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.)

RSREMD

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!