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:

 

To ensure that all aspects of site production operate within all established quality systems. You will support the cGMP and/or ISO 9001 quality systems such as training, batch record reviews and documentation control. Responsibilities and tasks include:

 

Safely perform operations to meet quality expectations.Improve quality systems in both GMP and ISO production and packaging environments.Drive quality improvement in multiple departmentsBe the “voice of quality” on the production and packaging floors performing routine walk through. o Review quality documents in production and packing areas.Assist Quality Team issuing and reviewing batch records for GMP manufacturing.Review ISO and GMP in-process batch records and form for good documentation.Communicate the status of operations and bring critical deviations to the attention of the appropriate parties.Communicate with coworkers and interact with other departments regularly.Complete and have accurate work consistently with quality guidelines.Take note of details and ensure others do as well.Assist in maintaining department KPIs through on time CAPAs, Deviations, and Complaints.Assist in compliance with Life Science and site quality policies and procedures.Ability to serve on committees to improve department, site, or company performance. Committees may focus on safety, quality, inventory, output, costs, etc.In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles.

 

Who You Are

 

Minimum Qualifications:

 

High School Diploma or GED2+ years of experience in a quality role at a GMP manufacturing facility

 

OR

 

Associate’s degree in any discipline. 1+ years of experience in a quality role at a GMP manufacturing facility.

 

Preferred Qualifications:

 

Bachelor's degree in chemistry, Biology, or other science discipline.Previous QA experience in a GMP manufacturing or testing facility.3-5 years’ work experience in a GMP Manufacturing Facility.Experience with quality management systems such as Trackwise, electronic document management systems, etc.Ability to multitask and prioritize.Understanding of ISO and cGMP quality standards.Computer literacy, including Microsoft Word and Excel.

 

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!