Quality Assurance Associate at Millipore Corporation in Lenexa, Kansas

Job Description:

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 at MilliporeSigma in Lenexa will ensure that all aspects of product manufactured meet production, packaging, labeling, and test specifications in accordance with established quality systems. Support the maintenance, development, and improvement of quality systems, such as auditing, training, and change control. Make batch release determination and generate CoA and other specified batch documents.



Your Role:

• Review and release of raw materials in a timely manner, assuring any lot deviations and Out of Specifications (OOS) are completed and closed


• Performing label approval, label generation, and review of daily QA paperwork to include charts, monitoring exhibits, and environmental records, and reviewing batch records prior to production use


• Participate in cross-functional deviation investigations, root cause analysis, and CAPA plan development, maintaining CAPA tracking and performing effectiveness check as applicable


• Assisting in customer audits including document reviews and any follow-up activities as necessary


• Assist periodic internal audits to meet corporate and ISO/EXCiPACT requirements


• Takie part in and contributing to a safe working environment by following corporate and departmental safety regulations


• Manage Site Quality filing systems

Who You Are




Minimum Qualifications:

• Bachelor's Degree in Biology, Chemistry, or other Life Science discipline

OR

• High School Diploma or GED


• 1+ years in a Quality Assurance role in a GMP environment


• 2+ years of work experience in the Pharmaceutical, Biopharm, or other Healthcare industry

Preferred Qualifications:

• Knowledge of commercial Quality systems and their application in a manufacturing environment


• Excellent customer service skills and the ability to negotiate win-win outcomes

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 Apply Now