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GMP Packaging Technician Shift Lead-Nights

 

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 Lead 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.  

 

  • Lead GMP Packaging technicians by providing guidance and support in preparation, execution, and reconciliation of packaging, labeling, and Raw Material Sampling events.
  • Identify and resolve issues proactively, promoting a positive and collaborative work environment.
  • 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.)
  • Take action to resolve unsafe conditions.
  • Maintain required training to perform tasks/assignments and provide training to technicians as needed.
  • Maintain clean working areas during and after operations.
  • Utilize SAP in conjunction with packaging activities.
  • Ability to suggest effective corrective/preventative action.
  • Assist GMP Supervisor with adherence to the production schedule by ensuring that the necessary documentation, components, and support materials are available.
  • Act as a resource for the site’s continuous improvement culture by proposing and implementing ideas to reduce human error deviations and packaging improvements based on Lean Manufacturing principles.
  • Reports any significant activities to Supervisor in a timely manner.
  • Assists the Supervisor with projects and other duties as assigned.
  • Performs review of production documentation (MPFs, OPs, logbooks, etc.) for compliance and/or effectiveness.
  • Provide input in deviation investigations through interviews and support implementations of CAPA actions.
  • Work cross-functionally with Quality Control, Quality Assurance, Materials Management, Engineering, and Maintenance.
  • Must have the ability to simultaneously multi-task across multiple capabilities and functions and handle multiple competing priorities and requirements, including performing site and functional responsibilities, responding to email and phone communications, and attending meetings.

 

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.

 

This is an off-shift role involving flexibility as needed to meet manufacturing and production needs. Training will take place during the first shift hours of 6:00am-2:30pm for 3-4 months, then transition to Night shift Tuesday – Friday 10 hours shift starting at 5:30 pm.

 

Who You Are:

 

Minimum Qualifications:

 

  • High School Diploma or GED.
  • 2+ years of pharmaceutical packaging, industrial, or laboratory experience.

 Preferred Qualifications:

 

  • SAP knowledge.
  • Experience working with and in proximity of hazardous chemicals.
  • Experience with packaging labelling printing, including Zebra and LIMS.
  • Experience leading a team.
  • Legible handwriting and strong oral and written communication skills.
  • GMP knowledge.
  • Basic math skills including knowledge of the metric system.

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

 

Job Requisition ID:  279933
Location:  St. Louis
Career Level:  C - Professional (1-3 years)
Working time model:  full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

Notice on Fraudulent Job Offers
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