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Join a leading company in science and technology as a Production Lab Tech Lead in St. Louis, MO. You'll oversee production processes while ensuring quality and efficiency. This entry-level role requires strong communication and attention to detail, ideal for candidates passionate about making a difference in the life sciences industry.
1 week ago Be among the first 25 applicants
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
Responsibilities
Under moderate supervision and direction, the Production Lab Tech Lead completes and advises team members on tasks related to all production processes—including performing standard and new operating procedures, conducting area clearance tasks while maintaining separation of product, and collecting and recording data on documents and batch records where required. These responsibilities span filling, packaging, and labeling, which are performed independently with a high level of attention to detail and in accordance with GMP regulations. The Production Lab Tech Lead serves as a leader and Subject Matter Expert (SME) in their production area and is the go-to person for troubleshooting and problem solving across all Production work areas and tasks. Daily activities may also involve troubleshooting in SAP, supporting Dev/CAPA investigations, and maintaining lab cleanliness and safety. The lead 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:
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