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Cgmp Jobs (NOW HIRING)

Houston Methodist

The cGMP Technician position will perform basic maintenance tasks, ensuring equipment is in good working order. FLSA STATUS Exempt QUALIFICATIONS EDUCATION * Bachelor's degree or four years ...

CSBio

Manager, cGMP Manufacturing

Milpitas, CA · On-site

In 2023, we added additional cGMP clinical production capacity in Milpitas, CA. Position Summary As Manager of cGMP Peptide Manufacturing, you will lead our peptide production operations during a ...

CSBio

Manager, cGMP Manufacturing

Milpitas, CA

In 2023, we added additional cGMP clinical production capacity in Milpitas, CA. Position Summary As Manager of cGMP Peptide Manufacturing, you will lead our peptide production operations during a ...

CSBio

Manager, cGMP Manufacturing

Milpitas, CA · On-site

In 2023, we added additional cGMP clinical production capacity in Milpitas, CA. Position Summary As Manager of cGMP Peptide Manufacturing, you will lead our peptide production operations during a ...

Epicur

cGMP Warehouse Supervisor

Mount Laurel, NJ · On-site

$28/hr

Epicur follows Current Good Manufacturing Practices (cGMP) which are the same rules and regulations followed by commercial manufacturers. Epicur Pharma is proud to be a pioneer in animal drug ...

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How much do cgmp jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for cgmp in the United States is $34.14, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $40.87 per hour, depending on experience, location, and employer.

What is a cGMP job?

A cGMP job refers to a role that follows Current Good Manufacturing Practices (cGMP) in industries like pharmaceuticals, biotechnology, and food production. These jobs ensure products are consistently produced and controlled according to quality standards. Employees in cGMP roles follow strict guidelines for cleanliness, documentation, and compliance to maintain safety and efficacy. Common positions include quality assurance, manufacturing operators, and regulatory specialists.

What jobs pay 2000 a day?

High-paying jobs that can reach $2,000 a day often include specialized roles such as senior corporate executives, certain medical specialists, high-level consultants, and experienced freelance professionals in fields like software development or finance. These positions typically require advanced skills, extensive experience, and often involve project-based or contractual work. Earning this level of income usually depends on industry, location, and individual expertise.

What is the work of CGMP?

A CGMP (Current Good Manufacturing Practice) professional ensures that pharmaceutical, biotech, or food manufacturing processes comply with regulatory standards to produce safe and effective products. Their work involves quality control, documentation, and adherence to regulations set by agencies like the FDA, often requiring knowledge of quality systems and inspection procedures.

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

High-paying jobs that can reach $10,000 a month without a degree often include roles such as commercial pilots, real estate brokers, sales managers, and certain skilled trades like electricians or plumbers. Success in these fields typically depends on experience, certifications, or licensing rather than formal education, and they may require strong sales skills, technical knowledge, or entrepreneurial effort.

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

To thrive in a cGMP (Current Good Manufacturing Practices) role, you need a strong understanding of pharmaceutical or biotechnology manufacturing processes, quality control, and regulatory compliance, typically supported by a degree in life sciences or engineering. Familiarity with quality management systems (QMS), documentation protocols, and certifications like Six Sigma or cGMP training is highly beneficial. Attention to detail, teamwork, and strong communication skills are important for collaborating in cross-functional environments and ensuring compliance. These skills are critical for maintaining product safety, meeting regulatory standards, and supporting efficient manufacturing operations.

What are common challenges faced in cGMP roles within pharmaceutical manufacturing?

Professionals working in cGMP roles often encounter challenges such as maintaining strict compliance with regulatory standards and adapting to frequent updates in guidelines. Attention to detail is essential, as even small errors in documentation or process execution can have significant consequences for product safety and compliance. Team members must work effectively across departments like quality assurance, production, and regulatory affairs to troubleshoot deviations and implement corrective actions. Successful cGMP professionals embrace continuous learning and adaptability to thrive amidst evolving industry requirements and technologies.

What jobs in the US pay 300,000 a year?

For a Cgmp (Chief Good Manufacturing Practice) professional, high-paying roles typically include senior management positions in pharmaceutical or biotech manufacturing, such as Director or Vice President of Manufacturing, which can reach or exceed $300,000 annually with experience and bonuses. These roles often require extensive industry knowledge, leadership skills, and compliance expertise with GMP regulations. Other high-paying jobs in related fields include specialized pharmaceutical consultants and regulatory affairs directors.
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Cgmp jobs near you
Infographic showing various Cgmp job openings in the United States as of June 2026, with employment types broken down into 75% Full Time, 4% Part Time, 8% Contract, and 13% Nights. Highlights an 100% In-person job distribution, with an average salary of $71,008 per year, or $34.1 per hour.
cGMP technician

cGMP technician

Houston Methodist

Full-time

Posted 6 days ago

Houston Methodist rating

8.1

Company rating: 8.1 out of 10

Based on 293 frontline employees who took The Breakroom Quiz

70th of 872 rated healthcare providers

Job description

At Houston Methodist, the cGMP Technician position is responsible for supporting and assisting the production of therapeutics and medical devices by following Standard Operating Procedures (SOPs) and learning to apply current Good Manufacturing Practices (cGMP). Under the guidance of cGMP team members, this position will assist with compliance activities, verify equipment and facility cleanliness, accurately record data into relevant systems, receive, label, and process samples. The cGMP Technician position will perform basic maintenance tasks, ensuring equipment is in good working order. FLSA STATUS
Exempt
QUALIFICATIONS
EDUCATION
  • Bachelor's degree or four years' experience in lieu of a bachelor's degree

EXPERIENCE
  • Experience within a regulated environment (FDA, NIH, Instructional/Teaching facility) with exposure to cGMP manufacturing operations preferred

KNOWLEDGE AND ABILITIES
  • Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through ongoing skills, competency assessments, and performance evaluations
  • Sufficient proficiency in speaking, reading, and writing the English language necessary to perform the essential functions of this job, especially with regard to activities impacting patient or employee safety or security
  • Ability to effectively communicate with patients, physicians, family members and co-workers in a manner consistent with a customer service focus and application of positive language principles
  • Basic understanding of quality, compliance, and FDA regulatory principles, with an interest in learning Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP)
  • Proficiency in spreadsheet, word processing and presentation software
  • Ability to work under pressure and balance many competing priorities; highly responsive and solution/action oriented
  • Willingness to learn from and collaborate with experienced team members; open to feedback and coaching
  • General awareness of drug and device regulations (e.g., 21 CFR Parts 210/211, ICH guidelines) with a desire to deepen knowledge and apply it appropriately across different stages of development (GLP, Phase I-III)
  • Supports the preparation and delivery of pre-clinical and clinical materials in alignment with production schedules and quality expectations
  • Collaborates with cross functional teams including research, process development, quality assurance and quality control

ESSENTIAL FUNCTIONS
PEOPLE ESSENTIAL FUNCTIONS
  • Collaborates with all members of the cGMP team by actively communicating, providing meaningful contributions and reporting pertinent information as it relates to assigned system(s) in a comprehensive manner.
  • Works with research team members to assist them with transitioning their research processes to compliant cGMP SOPs.

SERVICE ESSENTIAL FUNCTIONS
  • Maintains accurate records of manufacturing processes.
  • Accurately entering data into relevant systems.
  • Participates in internal audits and external inspections by regulatory agencies.

QUALITY/SAFETY ESSENTIAL FUNCTIONS
  • Maintains laboratory equipment, ensuring it is in good working order, and performs basic maintenance tasks.
  • Assists in internal inspections and audits to ensure compliance with Federal Drug Administration (FDA) regulations and cGMP Core policies and procedures.
  • Assists with discrepancy inspections.

FINANCE ESSENTIAL FUNCTIONS
  • Uses resources efficiently; does not waste supplies.
  • Self-motivated to independently manage time effectively and prioritize daily tasks.

GROWTH/INNOVATION ESSENTIAL FUNCTIONS
  • Assists Quality Assurance Manager, cGMP Core Director and/or team members in developing and executing protocols, performing periodic updates and/or revisions to SOPs.
  • Seeks opportunities to expand learning beyond baseline competencies with a focus on continual development.
  • Supports Sr cGMP staff with ad-hoc projects as required.

SUPPLEMENTAL REQUIREMENTS
    WORK ATTIRE
    • Uniform: No
    • Scrubs: No
    • Business professional: Yes
    • Other (department approved): No

    ON-CALL*
    *Note that employees may be required to be on-call during emergencies (ie. Disaster, Severe Weather Events, etc) regardless of selection below.
    • On Call* No

    TRAVEL**
    **Travel specifications may vary by department**
    • May require travel within the Houston Metropolitan area No
    • May require travel outside Houston Metropolitan area No

Work Shift:

1 - Day (United States of America)

Job Category:

Non-clinical Houston Methodist is one of the nation's leading health systems and academic medical centers. The health system consists of eight hospitals: Houston Methodist Hospital, its flagship academic hospital in the Texas Medical Center, seven community hospitals and one long-term acute care hospital throughout the Greater Houston metropolitan area. Houston Methodist also includes a research institute; a comprehensive residency program; international patient services; freestanding comprehensive care clinics, emergency care and imaging centers; and outpatient facilities. Come lead with us!

Houston Methodist is an Equal Opportunity Employer.

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