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:  

 

At MilliporeSigma, as a Packaging Technician at our Cherokee site, you 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.  

 

Adhere to procedures consistent with, and established according to, current Good Manufacturing Practices.Prep for GMP packaging and labelling events that consists of MPF and label request, label review, labels kitting.Prepare Raw Material paperwork (ae. Bulk Sampling form, Sampling Line Clearance, SDS).Execute packaging, labelling, and raw material sampling events.Track direct event hours and components used using cost tracking sheets.Zebra label printing and LIMS printing.Generate TOs for materials and components if applicable.Print SAP Storage Unit Labels for finished goods as required.Order components using SAP and reconcile inventory through cycle count.Stock supplies and assure inventory is sufficient.Enter information into the Product History spreadsheet to accurately track the status of each product moving through the GMP Packaging group.Provide input in deviation investigations through interviews and support implementations of CAPA actions.Support Logbook management, documents and records review and editing.Keep training up to date and be Audit ready.Maintain departmental goals and objectives in a safe manner and in compliance with all applicable federal, state, and company regulations (OSHA, EPA, FDA, EMA etc.).Work cross-functionally with Quality Control, Quality Assurance, Materials Management, Engineering, and Maintenance.Support of any coordination of event.Maintain all 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. 6+ months of pharmaceutical packaging, industrial, or laboratory experience.

 

Preferred Qualifications

 

GMP knowledge.Experience working with and in proximity of hazardous chemicals and human source materials.SAP knowledge.Basic math skills including the metric system.Legible handwriting and strong oral and written communication skills.

 

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