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, as the Buffer Formulations Operator at our Cherokee Site/ 3300 S. Second Ave, St Louis, you 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. The primary responsibility will be creating buffer formulations in support of Drug Substance manufacturing.

The Formulations Operator is a key role within our GMP Manufacturing/Operations Systems & Support team.   Expectations is to ensure “Compliance“ and “Readiness” within our GMP Operations teams, ultimately enabling high manufacturing success. 

         

Prepare buffer formulations in support of Drug Substance manufacturing, with a focus on safety and quality.Maintain cleanliness of manufacturing areas including cleaning during regularly scheduled intervals (daily, weekly, etc.).Execution and documentation of daily tasks following current Good Manufacturing Practices (cGMPs).Utilize quality approved operating procedures and document activities with adherence to GDP standards.Maintaining logbooks in accordance with the procedure.Safely and properly dispose cleaning and process waste per approved procedures.Maintain safe stock of supplies and gowning utilizing Kanban system.Aid/input in quality deviations as needed.Perform safety inspections and necessary preventive maintenance.Assist in preparation of and follow procedures to ensure compliance with applicable Safety and Quality guidelines.Develop and assist in the implementation of process improvement, safety, quality, and 6STraining of new employees on department policy, procedure, and processes.Assist in a department functions and work closely with department supervisor to ensure daily department operating goals are achieved.This is a first shift role that may necessitate working evenings and weekends to fulfill production needs.

 

Physical Attributes:

 

Stand for extended periods of time.   Lift, 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 experience in a pharmaceutical GMP operations environment (Manufacturing, Quality, MSAT).

 

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 celebrate all dimensions of diversity and believe that it 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 our diverse team!

 

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html