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Gmp Manufacturing Jobs (NOW HIRING)

GMP Cleaning Associate

Germantown, MD · On-site

$45K - $55K/yr

Prior experience in cleaning GMP manufacturing areas and labs are required. GMP Cleaning Associate will maintain cleanliness in production, lab, and warehouse areas. This role focuses on adhering to ...

The GMP Mechanic works closely with Manufacturing, Engineering, Validation, Quality, Laboratory Operations, and Facilities to execute maintenance activities while maintaining compliance with cGMP ...

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How much do gmp manufacturing jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for gmp manufacturing in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What is a GMP manufacturing?

A GMP Manufacturing job involves producing pharmaceutical, biotechnology, or medical device products while following Good Manufacturing Practices (GMP) regulations. Responsibilities typically include operating equipment, maintaining sterile environments, documenting processes, and ensuring product quality and compliance. These roles are essential for maintaining safety and regulatory standards in healthcare-related manufacturing industries.

What are the key skills and qualifications needed to thrive in GMP manufacturing?

To excel in GMP Manufacturing, you need a solid understanding of Good Manufacturing Practices, attention to detail, and experience in regulated production environments, often backed by a degree in life sciences or engineering. Familiarity with quality management systems, batch record documentation, and equipment such as bioreactors or chromatography columns is typically required, and certifications like GMP or Six Sigma can be beneficial. Strong teamwork, communication skills, and the ability to follow precise procedures are essential soft skills for this position. These competencies ensure safe, compliant, and efficient production of pharmaceuticals or biotechnology products within strict regulatory frameworks.

What are some common challenges faced in GMP manufacturing roles?

Employees in GMP Manufacturing often encounter challenges such as maintaining meticulous documentation, adapting to changing regulatory requirements, and adhering to strict cleanliness and safety standards. The production process must be tightly controlled and deviations must be reported and resolved promptly, which requires a high level of diligence and accountability. Additionally, working collaboratively with quality assurance, engineering, and other cross-functional teams can add complexity to daily operations. Overcoming these challenges helps ensure product quality and regulatory compliance, while also providing valuable professional experience in one of the most highly regulated industries.

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What cities are hiring for Gmp Manufacturing jobs?

Cities with the most Gmp Manufacturing job openings:

What are the most commonly searched types of Gmp Manufacturing jobs?

The most popular types of Gmp Manufacturing jobs are:

What states have the most Gmp Manufacturing jobs?

States with the most job openings for Gmp Manufacturing jobs include:

Infographic showing various Gmp Manufacturing job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 4% Part Time, 3% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.

GMP Manufacturing Technician 4 - Night Shift

The businesses of Merck KGaA, Darmstadt, Germany

Saint Louis, MO • On-site

$24 - $41/hr

Full-time

Medical, Retirement, PTO

This job post has expired 3 days ago. Applications are no longer accepted.


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 Manufacturing Technician 4 - Night Shiftt 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 6:00pm - 6:30am including a 20% 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:

  • High school diploma or GED.
  • 6 months' experience in a pharmaceutical GMP operations environment (Manufacturing, Quality, MSAT, knowledge of Good Documentation Practices).

Preferred Qualifications:

  • Prior experience in pharmaceutical 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.)

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. For more information clickhere


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!

Employment Type: FULL_TIME