Quality Assurance Specialist - 2nd 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 Quality Assurance Associate provides compliance oversight across the St. Louis ISCO MilliporeSigma Quality Management System (QMS) in collaboration with site personnel.  As a QA Associate you are responsible for the coordination and maintenance of Quality Systems (i.e., Document Control, Record Control, Training Program Maintenance, Deviation/CAPA) and processes to ensure internal and external compliance and the promotion of quality practices that meet or exceed required guidelines and regulatory requirements. Responsibilities include maintenance and continuous improvement of the overall Quality Program.

• Shift :  Monday-Thursday 1:30pm - 12am  
• Improve quality systems in ISO and non-GMP production environments
• Documentation control activities include management of the electronic documentation management system, and the ability to write, review or approve Operation Procedures, Specifications, Master Manufacturing & Packaging Procedures and other controlled documents
• Training Management coordination including metric reporting and management of the electronic training platform. Complete a high volume of work to meet department goals
• Communicate with coworkers and interact with other departments on a regular basis
• Complete and have accurate work consistently with quality guidelines
• Assist in maintaining department KPIs through on time CAPAs, Deviations, Complaints and Change Controls
• Assist in compliance with Life Science and site quality policies and procedures
• Assist in internal audits
• Assist in the investigation of customer complaints
• Contribute to Root Cause Investigations & Effectiveness Checks of Nonconforming Incidents
• Conduct Quality System Training specific to job function

Who You Are:

Minimum Qualifications:

• Bachelors Degree in Biology, Chemistry, or other Life Science disicpline and 6+ months experience in a Quality role

OR

• Associatess Degree in any discipline and 3+ years industry experience in a experience in a Quality role

OR

• High School Diploma or GED and 5+ years industry experience in a experience in a Quality role

Preferred Qualifications:

• Experience with ISO 9001 and ISO 13485 and regulatory compliance issues

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!