Packaging Technician 4 - Night Shift

Merck • Saint Louis, MO

1d • $25 - $41 • Onsite

About The Position

At MilliporeSigma, as the GMP Packaging Technician 4 – Night 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: This is off shift role that in addition requires flexibility to fulfill Manufacturing/production needs. Training will take place during the first shift hours of 0600-1430 for 3-4 months, then transition to Night shift Tuesday – Friday 10 hours shift starting at 5:30 pm.

Requirements

• High School Diploma or GED
• 6+ months of GMP/GDP experience, pharmaceutical packaging, or laboratory experience
• Demonstrate basic math skills (including the metric system), legible handwriting, and strong oral and written communication abilities

Nice To Haves

• Experience working with and in proximity of hazardous chemicals and human source materials
• SAP knowledge

Responsibilities

• Adhere to procedures consistent with, and established according to, current Good Manufacturing Practices
• Documentation following GDP (Good Documentation Practices) guidelines
• Prepare 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 group
• Provide input in deviation investigations through interviews and support implementations of CAPA actions
• Achieve 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 Maintenance
• Provide support for event coordination and maintain packaging areas in an audit-ready state.

Benefits

• We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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!

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED