ZipRecruiter

Log In

1

Gmp Manufacturing Jobs (NOW HIRING)

Wheeler Bio, Inc.

Manufacturing Supervisor

Oklahoma City, OK · On-site

$56K - $76K/yr

We are in search of a proficient and seasoned Manufacturing Supervisor with expertise in GMP (Good Manufacturing Practice) environments, particularly in overseeing cell culture and downstream ...

The O'Connor Group

Head of Manufacturing

Thousand Oaks, CA · On-site

$130K - $180K/yr

Hands-on GMP manufacturing expertise, including deviation investigation, root-cause analysis, and process troubleshooting on the production floor * Data driven decision making, using experimental ...

Lancesoft Inc

Manufacturing Associate

Portsmouth, NH · On-site

... GMP manufacturing facility Support the manufacturing floor for any process related questions Assist manufacturing change owner for changes impacting the process Ensure a quality and compliant ...

TekWissen LLC

Manufacturing Associate

Houston, TX · On-site

$20 - $24/hr

Perform Environmental Monitoring (EM) activities in support of GMP manufacturing of viral therapies * Support production and aseptic processing, including cell culture and product purification, when ...

next page

Showing results 1-20

All JobsGmp Manufacturing Jobs

Gmp Manufacturing information

See salary details

$13

$24

$34

How much do gmp manufacturing jobs pay per hour?

As of Jun 13, 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 GMP in manufacturing?

GMP in manufacturing stands for Good Manufacturing Practice, which are regulations that ensure products are consistently produced and controlled according to quality standards. For GMP manufacturing roles, knowledge of quality control, sanitation, and compliance with regulatory guidelines such as FDA standards is essential. These practices help prevent contamination, mix-ups, and errors in the production process.

What is a GMP Manufacturing job?

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 jobs pay 2000 a day?

In GMP manufacturing, high-paying roles such as senior process engineers, manufacturing directors, or specialized quality assurance managers can earn around $2,000 per day, especially with extensive experience, certifications, and leadership responsibilities. These positions often require advanced technical skills, industry knowledge, and sometimes overtime or shift work to reach such compensation levels.

What are the key skills and qualifications needed to thrive in the Gmp Manufacturing position, and why are they important?

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.

What profession makes $400,000 a year?

In GMP manufacturing, senior roles such as manufacturing directors, quality assurance directors, or regulatory affairs managers can earn $400,000 or more annually, especially with extensive experience, advanced certifications, and leadership responsibilities. These positions often require strong technical knowledge, management skills, and industry experience in pharmaceutical or biotech production environments.

What jobs pay $10,000 a month without a degree?

In GMP manufacturing, high-paying roles such as process engineers, quality managers, or senior production supervisors can reach or exceed $10,000 per month, often requiring specialized skills, experience, and industry certifications. These positions typically involve overseeing manufacturing processes, ensuring compliance, and optimizing production efficiency, with some roles offering high compensation based on expertise and responsibility.
More about Gmp Manufacturing jobs
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:
What job categories do people searching Gmp Manufacturing jobs look for? The top searched job categories for Gmp Manufacturing jobs are:
Gmp Manufacturing jobs near you
Infographic showing various Gmp Manufacturing job openings in the United States as of June 2026, with employment types broken down into 1% Internship, 50% Full Time, 42% Part Time, 3% Temporary, 2% Contract, and 2% Nights. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.
Manufacturing Supervisor

Manufacturing Supervisor

Wheeler Bio, Inc.

Oklahoma City, OK • On-site

$56K - $76K/yr

Full-time

Posted 11 days ago

Job description

Manufacturing Supervisor

POSITION SUMMARY:

We are in search of a proficient and seasoned Manufacturing Supervisor with expertise in GMP (Good Manufacturing Practice) environments, particularly in overseeing cell culture and downstream processing operations. The ideal candidate should possess over 6 years of relevant experience, demonstrating a strong proficiency in cell culture techniques and a track record of ensuring adherence to quality standards. As an integral part of our manufacturing leadership team, you will be instrumental in driving the production of top-tier biopharmaceutical products.

RESPONSIBILITIES:

· Oversee and supervise GMP manufacturing processes for cell culture-based production, ensuring strict compliance with established protocols and regulatory standards.

· Lead routine tasks such as media preparation, cell inoculation, bioreactor operation, and harvest operations, ensuring meticulous execution and adherence to quality parameters.

· Foster collaboration with cross-functional teams, including Quality Control and Quality Assurance, to uphold product quality and regulatory compliance.

· Spearhead troubleshooting efforts and resolution of process deviations, conducting root cause analyses and implementing corrective measures to optimize manufacturing efficiency.

· Maintain comprehensive documentation of all manufacturing activities in accordance with GMP standards, ensuring the accuracy and completeness of batch records and related documentation.

· Play a pivotal role in technology transfer activities, leveraging expertise in cell culture processes to contribute to process enhancement initiatives.

· Facilitate the training and development of junior team members, actively participating in the formulation of standard operating procedures (SOPs) pertaining to cell culture manufacturing.

· Ensure the upkeep of equipment and work areas in accordance with safety protocols and guidelines, fostering a culture of safety and compliance.

PROFESSIONAL SCOPE:

· JOB LEVEL: Assumes responsibility for developing professional expertise, applying company policies and procedures to resolve various issues.

· EXPERIENCE: Typically necessitates a university degree and a minimum of 8 years of relevant experience in a managerial or supervisory capacity.

· COMPLEXITY: Deals with challenges of moderate scope, requiring analysis of diverse factors. Exercises judgment within defined procedures and practices, fostering productive internal and external relationships.

· SUPERVISION: Generally receives general instructions for routine tasks, while detailed instructions are provided for new projects or assignments.

LOCATION:

Wheeler Bio's headquarters are situated in Oklahoma City, OK. The selected individual is expected to operate onsite, necessitating relocation to the Oklahoma City headquarters to oversee this expanding team effectively.

CANDIDATE QUALIFICATIONS:

· Bachelor's degree in a pertinent scientific discipline (Biotechnology, Biochemistry, Biology, or a related field) preferred.

· Over 8 years of hands-on experience in GMP manufacturing, with a specialized focus on cell culture processes.

· Profound understanding of bioreactor operations, aseptic techniques, and upstream processing. Experience with tangential flow filtration, ultracentrifugation and bulk fill downstream operations is a plus.

· Hands-on experience with the Thermo Fisher DynaDrive STR system preferred, or comparable STR platforms.

· Familiarity with regulatory requirements governing the production of biopharmaceuticals, including FDA and EMA guidelines.

· Exceptional problem-solving and analytical aptitude, coupled with the capacity to troubleshoot and refine manufacturing processes.

· Strong communication and collaboration skills, enabling effective interaction across departments and fostering a positive team dynamic.

· Detail-oriented with a demonstrated ability to maintain meticulous documentation in compliance with GMP standards.