GMP Associate Production Scientist - Day Shift

MilliporeSigma; St. Louis (MO); On-site; USD 34,440 - 56,481; Full time

Benefits offered by this job

Health insurance

Paid time off (PTO)

Retirement contributions

Bonus potential

Job summary

MilliporeSigma is hiring a GMP Associate Production Scientist for the Day Shift at the Cherokee site in Missouri. The role focuses on manufacturing products per validated protocols, supporting the team, and maintaining quality records in a fast-paced environment.

Ideal candidates bring a science degree (or equivalent) and 2+ years of GMP production experience, with strong documentation skills and familiarity with lab instruments.

Qualifications

• Bachelor’s degree in a science field or an associates degree with GMP production experience.
• 2+ years in pharmaceutical GMP operations, including quality systems and documentation.
• Familiarity with laboratory instruments and process techniques.

Responsibilities

• Manufacture products per established protocols and provide technical support.
• Support 24/7 manufacturing operations with 12‑hour shifts and 5% differential.
• Maintain complete and accurate records per quality guidelines.
• Assist with buffer formulation and communication with ADC.

Skills

GMP experience

Good Documentation Practices

Quality mindset

Education

Bachelor’s Degree in Chemistry/Biochemistry/Biology

Associate Degree in Chemistry/Biochemistry/Biology

Tools

Microsoft Office

Job description

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 Associate Production Scientist – Day Shift at the 3300 South Second Ave/ Cherokee site, will manufacture products according to established protocols, provide technical support to others and perform operations supporting the group and department. 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
• Evaluate products according to established protocols, provide technical support to others, and perform operations in support of the group and department.
• Safely perform operations to meet quality expectations.
• Assist with Buffer formulation Schedule and communication with ADC
• Maintain required training to perform tasks/assignments.
• Perform routine processes and unit operations.
• Clean equipment and working areas during and after operations.
• Support facility functions (e.g., maintain equipment, prepare reagents, restock supplies, waste disposal).
• Communicate the status of operations and convey concerns to the supervisor.
• Provide complete and accurate records consistent with quality guidelines.
• Ensure all applicable logbooks are completed as required by current procedures.
• Interact with other departments as needed and perform procedures independently and as part of a team.
• Participate as needed in quality audits and customer interactions.
• Improve processes by applying scientific knowledge, experience, and principles, in compliance with change control.
• Take action to resolve unsafe conditions.
• Train team members and act as technical consultants.

Physical Attributes

• Lift up to 35 lb
• Personal protective equipment such as a respirator or chemical protective clothing for extended periods.

Who You Are

Minimum Qualifications

• Bachelor’s Degree in Chemistry, Biochemistry, Biology, or other science disciplines

OR

• Associate Degree in Chemistry, Biochemistry, Biology, or other science discipline
• 2+ years of production, GMP experience (pharmaceutical GMP operations environment, Quality, knowledge of Good Documentation Practices).

Preferred Qualifications

• Familiar with laboratory instruments and production equipment
• Knowledge of process techniques, unit operations, and safe chemical handling methods.
• Experience with Microsoft Office (Word, Outlook, Excel, etc.).
• Mechanical and troubleshooting skills.
• Knowledge of ICH Regulatory and Quality standards.
• Knowledge of Operational Excellence.

RSREMD

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.

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!