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How much do cgmp jobs pay per hour?

As of Jul 6, 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 GMP for jobs?

GMP in a job context typically refers to Good Manufacturing Practice standards, which are regulations ensuring products are consistently produced and controlled according to quality standards. Jobs related to GMP often involve roles in pharmaceutical, biotech, or food manufacturing industries, requiring adherence to strict protocols, documentation, and sometimes specific certifications. Compliance with GMP is essential for maintaining product safety and quality.

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 can you do with a pharmaceutical chemistry degree?

A pharmaceutical chemistry degree prepares individuals for roles such as pharmaceutical chemist, formulation scientist, quality control analyst, or research scientist in the pharmaceutical industry. These positions involve drug development, synthesis, testing, and ensuring product safety and efficacy, often requiring laboratory skills and knowledge of regulatory standards.

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 is the highest paying pharmaceutical job?

In the pharmaceutical industry, senior roles such as Vice President of Pharmaceutical Development or Chief Scientific Officer typically have the highest salaries. These positions require extensive experience, advanced degrees, and leadership skills, often offering compensation exceeding $200,000 annually, sometimes including bonuses and stock options.

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 GMP Officer or similar high-level role), salaries of $300,000 or more are typically found in executive positions within the pharmaceutical or biotech industries, especially for those overseeing manufacturing compliance, quality assurance, or regulatory affairs. These roles often require extensive experience, advanced certifications, and leadership skills, and may include bonuses or stock options that contribute to total compensation.
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What cities are hiring for Cgmp jobs? Cities with the most Cgmp job openings:
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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 90% Full Time, 1% Part Time, 1% Temporary, 6% Contract, and 2% Nights. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $71,008 per year, or $34.1 per hour.
Construction Manager - Owner's Representative (cGMP Plant Expansion)

Construction Manager - Owner's Representative (cGMP Plant Expansion)

America At Work

Fresno, CA • On-site

$150K - $180K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 20 days ago

Job description

Lead a High-Profile cGMP Manufacturing Expansion
Our client is seeking an experienced Construction Manager / Owner's Representative to oversee construction activities for a major plant expansion project at a regulated cGMP manufacturing facility near Fresno, California.
This is a unique opportunity to represent the owner's interests on a high-visibility capital project while collaborating with engineering, construction, commissioning, and operations teams. The ideal candidate is a hands-on construction leader with extensive experience managing contractors, driving project execution, and ensuring alignment with safety, quality, schedule, and budget objectives.
If you thrive in complex industrial environments and enjoy being the key decision-maker in the field, we want to hear from you.
#Construction Manager #Owner's Representative $Capital Projects #Industrial Construction #Pharmaceutical Construction #cGMP # Life Sciences #Manufacturing Expansion #Plant Expansion #Field Construction Manager #Commissioning #Startup #Validation # General Contractor Management #Construction Execution #Project Controls #EPC, #industrial Facilities # Chemical Manufacturing #Biotechnology #FDA-Regulated Facilities, #Resident Engineer #Site Construction Lead.
What You'll Do
As the Owner's Representative, you will serve as the primary onsite liaison between the facility owner, general contractor, engineering team, and project stakeholders.
Key Responsibilities
  • Represent the owner during all phases of construction execution
  • Monitor and oversee field activities performed by the General Contractor and subcontractors
  • Ensure compliance with project safety standards, quality requirements, schedule milestones, and budget objectives
  • Track construction progress and proactively identify risks, delays, and execution challenges
  • Coordinate and facilitate timely resolution of RFIs, submittals, field issues, and design clarifications
  • Support planning and execution of construction work packages and contractor activities
  • Coordinate delivery, storage, installation, and startup readiness of owner-furnished equipment
  • Collaborate with project controls and scheduling teams to maintain the master project schedule
  • Interface with engineering, procurement, commissioning, validation, and operations personnel
  • Participate in project meetings and provide regular status updates to executive stakeholders
  • Assist with turnover, commissioning, startup, and project closeout activities

Required Qualifications
  • 8+ years of experience in Construction Management, Capital Projects, Field Execution, or Industrial Project Delivery
  • Experience managing construction activities on industrial, manufacturing, pharmaceutical, chemical, food processing, biotechnology, or life sciences projects
  • Strong understanding of:
    • Construction sequencing
    • RFIs and submittals
    • Contractor management
    • Scheduling and project controls
    • Field coordination
    • Quality assurance and safety programs
  • Proven ability to build relationships and influence General Contractors and project stakeholders
  • Strong communication, leadership, and problem-solving skills
  • Ability to work onsite near Fresno, CA for the duration of the project
  • Valid driver's license
  • Authorization to work in the United States without sponsorship

Preferred Qualifications
  • Experience serving as an Owner's Representative
  • Experience supporting cGMP, FDA-regulated, pharmaceutical, biotechnology, or life sciences facilities
  • Experience with commissioning, startup, turnover, and validation activities
  • Bachelor's degree in Construction Management, Engineering, Architecture, or a related discipline
  • PMP, CCM, OSHA 30, or similar industry certifications are highly desirable

Compensation & Benefits
  • Base Salary: $150,000 - $180,000 annually
  • $215/day Per Diem
  • Paid overtime as project demands require
  • Medical, Dental, and Vision Insurance
  • 401(k) with Company Match
  • Health Savings Account (HSA) Contributions
  • Paid Time Off (PTO)
  • Paid Holidays
  • Professional Development Opportunities

Ideal Backgrounds
We encourage applications from professionals currently serving as:
  • Construction Manager
  • Senior Construction Manager
  • Owner's Representative
  • Resident Engineer
  • Field Construction Manager
  • Capital Projects Manager
  • Industrial Construction Manager
  • Pharmaceutical Construction Manager
  • Life Sciences Construction Manager
  • Project Manager - Industrial Construction
  • Site Construction Lead
  • Commissioning & Construction Manager

$150,000 - $180,000 a year
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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