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:  

At MilliporeSigma, as the GMP Packaging Technician 4 - 1st Shift at our Cherokee site, will play a key role within our GMP Operations Systems & Support team.  This team supports Manufacturing through various functions including buffer manufacturing, training, compliance, equipment and facility cleaning, and raw material sampling.  Expectations of the GMP Operations System & Support team are to ensure compliance and readiness within our GMP Manufacturing teams, ultimately enabling high manufacturing success.  Job duties include:

Shift hours: Monday – Friday – 1st shift, with on call hours off shift as business needs requireAdhere to procedures consistent with, and established according to, current Good Manufacturing PracticesDocumentation following GDP(Good Documentation Practices) guidelinesPrepare Raw Material paperwork (ae. Bulk Sampling form, Sampling Line Clearance, SDS)Prepare for GMP packaging and labeling events (including MPF and label request, label review, and label kitting) and execute packaging, labeling, and raw material sampling events.Track direct event hours and component usage (via cost tracking sheets) and perform various printing tasks, including Zebra labels, LIMS documents, and SAP Storage Unit Labels for finished goods as required.Manage inventory sufficiency (including stocking supplies and assuring adequate levels), order components via SAP, reconcile inventory through cycle count, and generate TOs for materials/components as applicable.Enter information into the Product History spreadsheet to accurately track the status of each product moving through the GMP Packaging groupProvide input in deviation investigations through interviews and support implementations of CAPA actionsAchieve departmental goals and objectives safely and in compliance with all applicable regulations (e.g., FDA, OSHA), maintaining up-to-date training and audit readiness, and collaborating cross-functionally with departments such as QC, QA, Materials Management, Engineering, and MaintenanceProvide support for event coordination and maintain packaging areas in an audit-ready state.  

Physical Attributes:

Stand for extended periods of time.Lift, push, and or pull up to 50lbs.Wear mask, safety shoes, gloves, Tyvek suits, respirator, and related personal protective equipment

 

Who You Are:

Minimum Qualification:

High School Diploma or GED 1+ years' experience in a packaging / pharmaceutical operations environment

Preferred Qualifications:

GMP and GDP experienceExperience working with and in proximity of hazardous chemicals and human source materialsSAP knowledgeDemonstrate basic math skills (including the metric system), legible handwriting, and strong oral and written communication abilities

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