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.  

 

Your Role:

 

The Project Associate is responsible for assisting the Quality Control Management in oversight of operations within the Quality Control group. Responsibilities include leading or coordinating projects within safety, quality, scheduling, stability, metrics, regulatory and testing. Specific responsibilities include:

 

Coordinating the product shelf-life stability program including:              Scheduling of stability testingDocument preparation including protocols and summary reportsRoutine coordination of QC testing to support production schedules including:Testing and schedule entry into Quality Control Management System (QCMS)Regular QC and cross-functional team communications for workflow prioritization to ensure testing meets lab goals and established timelinesTest plan and batch record creation and revisionProject management of:Method, instrument and computer data system qualifications and validationsLab advancement initiativesCorrective Action Preventative Action (CAPA), deviation and change controlCoordinate completion of OOT and OOS investigations and actionsReview of product, raw material and custom analytical testing records for accuracy, completeness, and compliance for release to Quality Assurance reviewSchedule production and stability projects for testing to avoid backorders and supply distribution This includes:Timely scheduling of projects into QCMS in accordance with production and customer needsReview and revision of test plansAssigning appropriate due datesManage retest and stability programCollaborating with QC management to develop QC strategies and plans to optimize group performanceTimely review of finished product and validation recordsCoordinate thorough and timely completion of OOT and OOS investigations and associated action itemsIdentify quality issues and alerting managementLead or coordinating special projects and initiatives to improve QC lab safety, production and qualityPerforming other duties as assigned by the Lab Manager

 

 

Who You Are:

 

Basic Qualifications:

 

Bachelor’s Degree in Chemistry, Chemical Engineering, or other Life Science discipline2+ years of quality control experience

 

Preferred Qualifications:

 

Working knowledge of the ISO 9001, 17025 and 17034Working knowledge of GxP (GLP/GMP)

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