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, Manufacturing Support Technician 4 – 1st Shift at our Cherokee Site/ 3300 S. Second Ave, St Louis, will be expected to safely execute, develop new approaches, and perform support operations in a cGMP regulated environment for the support of API (Active Pharmaceutical Ingredients) manufacturing teams, including maintaining equipment, preparation of solutions, staging of equipment and supplies, and other various manufacturing support activities.  Job duties include:

 

Shift Hours: Monday – Friday, 9:30am – 6:00pm, flexibility with hoursEvaluate products according to established protocols and perform operations in support of the group and departmentSafely perform operations to meet quality expectations. Safely and properly dispose cleaning and process waste per approved proceduresMaintain required training to perform tasks/assignmentsClean equipment and working areas during and after operationsSupport 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 supervisorProvide complete and accurate records consistent with quality guidelines. Utilize quality approved operating procedures and document activities with adherence to GDP standardsEnsure all applicable logbooks are completed as required by current proceduresInteract with other departments as needed and performs procedures independently and part of a teamImprove processes through application of experience and principles, in compliance with change controlDevelop and assist in the implementation of process improvement, safety, quality, and 6STake action to resolve unsafe conditions

 

Physical Attributes  

Stand for extended periods of timeLift, push, and or pull up to 50lbs.Wear mask, 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 pharmaceutical GMP operations environment (Manufacturing, Quality, MSAT) 

Preferred Qualifications:

GDP experiencePrior experience in an API manufacturing environmentStrong mechanical aptitudeDemonstrated process improvement experienceFamiliarity with FDA, EMA, and other regulatory standardsDemonstrated 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!