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

 

Under direct supervision at our Spruce Site, the Production Lab Tech II performs technical duties in manufacturing, filling, labeling, packaging, shipping, and other lab-related tasks. Work is performed in accordance with standard operating procedures and includes basic laboratory techniques, calculations, material measurements, equipment operation, and record-keeping. Daily activities may also involve troubleshooting in SAP, supporting Dev/CAPA investigations, and maintaining lab cleanliness and safety.

Key responsibilities include verifying data, filling and labeling products according to the production plan, and using standardized methods. The role requires stocking inventory, adhering to safe lab practices, and supporting 6S Lean initiatives. The technician must comply with cGMP, FDA, OSHA, EPA, and Quality System regulations, and report any deviations to management. Additional duties include participating in failure investigations, attending meetings, composing professional emails, and presenting DMS Boards. The role follows site-specific standards such as MDSAP, ISO 13485, IVDR, and the site Quality Manual. Strong communication, customer service, and professionalism are essential. Specific responsibilities include:

 

Perform area clearance tasks and maintaining separation of productPerform standard and new operating proceduresCollect and record data on documents and batch records where requiredUtilize computer hardware and software for data entry and record keeping where requiredEnsure compliance with all Quality and Regulatory specificationsSupport process improvement through identification and reporting of areas needing improvement and assisting in improvement projectsEffectively utilize Quality Management Systems (QMS) and other applicable databasesFamiliarity with and proper use of safety equipment and Personal Protective Equipment (PPE)

 

Who You Are

 

Minimum Qualifications:

 

High school diploma or GED required1+ years of within a production or manufacturing environment 

 

Preferred Qualifications:

 

Working knowledge of SAP, SAP NEXT, or other ERP systems Knowledge of GMP facility, FDA QSRs, and ISO 13485Experience in an FDA regulated biotechnology or pharmaceutical environmentThe ability to learn, understand, and carry out safe laboratory practicesProficiency with Quality Management Systems (QMS) Knowledge of the metric systemsCommunicate effectively with all levels within the organization and with outside contacts

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