Manufacturing Technician 4 - 2nd 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:

At MilliporeSigma, as the Manufacturing Technician 4 – 2nd Shift at our Cherokee Site/ 3300 S. Second Ave, St Louis site you will be expected to safely execute, develop new approaches, and perform support operations in a cGMP regulated environment for the support of API (Active Pharmaceutical Ingredients) manufacturing teams, including maintaining equipment, preparation of solutions, staging of equipment and supplies, and other various manufacturing support activities. The primary responsibility will be creating buffer formulations in support of Drug Substance manufacturing. Job duties include:

• Shift Hours:  2nd shift, Monday – Friday, 2:00pm – 10:30pm, including a 10% shift differential


• Prepare buffer formulations in support of Drug Substance manufacturing, focusing on safety and quality, and maintain manufacturing area cleanliness through scheduled cleaning activities.


• Execute daily tasks in accordance with cGMPs and quality approved operating procedures, accurately documenting all activities (including maintaining logbooks) in adherence to GDP standards.


• Safely and properly dispose cleaning and process waste according to approved procedures and maintain safe stock levels of supplies and gowning using the Kanban system.


• Maintain compliance with applicable Safety and Quality guidelines through procedure adherence, assisting in their preparation, performing safety inspections and necessary preventive maintenance, and aiding/inputting in quality deviations as needed.


• Support department operations and goal achievement by training new employees on policies and procedures, assisting with daily functions, and contributing to the development and implementation of process improvement, safety, quality, and 6S initiatives, collaborating closely with the department supervisor. 

Physical Attributes:

• Stand for extended periods of time.   


• Lift, push, and pull up to 50lbs.  


• Wear mask, safety shoes, gloves, Tyvek suits, respirator, and related personal protective equipment.

Who you are

Minimum Qualifications:

• High school diploma or GED.


• 1 + years’ experience in a pharmaceutical GMP operations environment (Manufacturing, Quality, MSAT, Buffers).

Preferred Qualifications:

• Prior experience in an API manufacturing environment.


• Strong mechanical aptitude.


• Experience in GDP


• Demonstrated process improvement experience.


• Familiarity with FDA, EMA, and other regulatory standards.


• Demonstrated knowledge and experience in various computer skills, including Windows (Word, Excel, PowerPoint, etc

Pay Range for this position: $24.00 - $41.00.

Our ranges are derived from several sources, and largely reliant on relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career level, and other job-related factors.  This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k)-matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses

RSREMD

What we offer: 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!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!