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:

Ensure that all aspects of product manufacture meet production, packaging, labeling, and test specifications in accordance with established quality systemsSupport the maintenance, development, and improvement of quality systems, such as auditing, training, and change controlMake batch release determination and generate CoA and other specified batch documents.Perform review and release of raw materials and finished products in a timely mannerAssure any lot deviations and Out of Specifications (OOS) are completed and closedPerform label approval, label generation, and review of daily QA paperwork to include charts, monitoring exhibits, and environmental recordsReview batch records prior to productionAnswer questions from internal and external customersParticipate in and lead cross-functional deviation investigations, root cause analysis, and CAPA plan development, maintaining CAPA tracking and performing effectiveness check as applicableAssist in customer audits including opening/closing meetings, tours, document reviews and any follow-up activities as necessaryAssist in periodic internal audits to meet corporate and ISO/EXCiPACT requirementsApprove masterbatch records and batch records, assuring accuracy and completeness and resolve any discrepancies in documentationTake part in and contributing to a safe working environment by following corporate and departmental safety regulationsPerform new hire and ISO/EXCiPACT trainingMaintain Site Quality filing systems

 

Who you are:

Minimum Qualifications:

Bachelor’s Degree in Chemistry, Biology, or other Life Sciences discipline 1+ year direct Quality Assurance experience in a GMP environment2+ years of experience in a Pharmaceutical, Biopharm, or other Healthcare environment

OR

High School Diploma or GED1+ year direct Quality Assurance experience in a GMP environment4+ years of experience in a Pharmaceutical, Biopharm, or other Healthcare environment where they used cGMPs, cGLPs, ISO, and/or EXCIPACT requirements

Preferred Qualifications:

Experience using QMS software such as TrackWise or SAP QNQuality Auditor Certification or the ability to obtain certificationAn understanding of commercial Quality systems and their application in a manufacturing environmentExcellent customer service skills and the ability to negotiate win-win outcomesExperience as an auditor of supplier products and services

 

 

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