GMP Manufacturing Technician 4- Day Shift

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:
The GMP Manufacturing Technician 4 - Day Shift at MilliporeSigma's Cherokee Site (3300 S. Second Ave, St. Louis), you will play a key role in supporting API (Active Pharmaceutical Ingredients) manufacturing within a cGMP-regulated environment. This role is responsible for safely carrying out established procedures, contributing to the development of improved operational approaches, and providing essential manufacturing support. Day-to-day activities will encompass equipment maintenance, solution preparation, equipment and supply staging, and a variety of other manufacturing support tasks. Expectations to ensure “Compliance “and “Readiness” within our GMP Operations teams, ultimately enabling high manufacturing success. Job duties include:
Shift Details: This role will support 24/7 manufacturing operations and work 12-hour shifts from 6:00am – 6:30pm. including a 5% shift differential.
Prepare buffer formulations in support of Drug Substance manufacturing, with a focus on safety and quality.
Maintain cleanliness of manufacturing areas including cleaning during regularly scheduled intervals (daily, weekly, etc.).
Execution and documentation of daily tasks following current Good Manufacturing Practices (cGMPs).
Utilize quality approved operating procedures and document activities with adherence to GDP standards.
Maintaining logbooks in accordance with the procedure.
Safely and properly dispose cleaning and process waste per approved procedures.
Maintain safe stock of supplies and gowning utilizing Kanban system.
Aid/input in quality deviations as needed.
Perform safety inspections and necessary preventive maintenance.
Assist in preparation of and follow procedures to ensure compliance with applicable Safety and Quality guidelines.
Develop, assist in the implementation of process improvement, safety, quality, and 6S
Training of new employees on department policy, procedure, and processes.
Assist in a department function and work closely with department supervisor to ensure daily department operating goals are achieved.
Physical Attributes:
Stand for extended periods of time.
Lift, push, and or pull up to 35lbs.
Wear mask, safety shoes, gloves, Tyvek suits, respirator, and related personal protective equipment.
Who you are:
Minimum Qualifications: