GMP Manufacturing Technician 4 - 2nd Shift
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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, Manufacturing and Facility Cleaning Support Technician 4 – 2nd Shift at our Cherokee Site/ 3300 S. Second Ave, St Louis, 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. Job duties include:
Shift Hours: Monday – Friday, 2:00pm – 10:30pm, including a 10% shift differential
Clean manufacturing equipment and facilities before, during and after operations
Support functions of the facility (e.g., maintain equipment, prepare cleaning solutions, and restock supplies, waste disposal)
Safely perform operations to meet quality expectations. Safely and properly dispose cleaning and process waste per approved procedures
Maintain required training to perform tasks/assignments
Support functions of the facility (e.g., maintain equipment, prepare reagents, and restock supplies, waste disposal)
Communicate the status of operations and convey concerns to the supervisor
Provide complete and accurate records consistent with quality guidelines. Utilize quality approved operating procedures and document activities with adherence to GDP standards
Ensure all applicable logbooks are completed as required by current procedures
Interact with other departments as needed and performs procedures independently and part of a team
Improve processes through application of experience and principles, in compliance with change control
Develop and assist in the implementation of process improvement, safety, quality, and 6S
Take action to resolve unsafe conditions
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.
6 + months of experience working in a pharmaceutical GMP operations environment (Manufacturing, Quality, MSAT)
Preferred Qualifications:
GDP experience
Prior experience in an API manufacturing environment
Strong mechanical aptitude
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.
2 + years of experience working in a pharmaceutical GMP operations environment (Manufacturing, Quality, MSAT)
Pay Range for this position: $24.00 - $41.00
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here .
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!
Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 3428 comparable Manufacturing & CMC roles across 175 biopharma companies.
Salary context
812 of 3428 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 3428 comparable roles
+ 55 more countries
Seniority mix
1516 of 3428 peers have a known seniority level
Therapeutic area mix
22 of 3428 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
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How we calculate "similar"
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.