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Part Time Gmp Auditor Jobs (NOW HIRING)

Eliquent Life Sciences, Inc

Consultant 1

Montrose, CA · On-site

Execute validation testing and document results in compliance with GMP/GLP standards. * Support ... Attractive salary and comprehensive benefits package for full-time and part-time employees ...

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Certified Group

Part-time Courier

Dallas, TX · On-site

$15.50 - $19.75/hr

FSNS Certification & Audit - Provides accredited third-party auditing and certification services, including food safety, animal welfare, and GMP programs. Job Summary The Courier I is responsible for ...

Certified Group

Part Time Lab Analyst

Springdale, AR · On-site

FSNS Certification & Audit - Provides accredited third-party auditing and certification services, including food safety, animal welfare, and GMP programs. Job Summary: Perform analytical and ...

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Part Time Gmp Auditor information

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$10

$19

$46

How much do part time gmp auditor jobs pay per hour?

As of Jul 4, 2026, the average hourly pay for part time gmp auditor in the United States is $19.21, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Part Time GMP Auditor, and why are they important?

To thrive as a Part Time GMP Auditor, you need in-depth knowledge of Good Manufacturing Practices, regulatory compliance, and quality management systems, typically supported by a background in life sciences or a related field. Familiarity with audit management software, documentation systems, and relevant certification such as ISO or GMP auditor credentials is highly valued. Strong attention to detail, analytical thinking, and effective communication are crucial soft skills for conducting thorough audits and delivering clear findings. These skills ensure that organizations maintain compliance, minimize risks, and uphold product quality and safety standards.

What is the difference between Part Time Gmp Auditor vs Part Time Gmp Inspector?

AspectPart Time Gmp AuditorPart Time Gmp Inspector
CertificationsGMP Auditor Certification, relevant quality assurance credentialsGMP Inspector Certification, quality control training
Work EnvironmentAuditing manufacturing facilities, documentation reviewInspecting production lines, on-site compliance checks
Employer & Industry UsagePharmaceutical, biotech, and supplement companiesRegulatory agencies, manufacturing plants

While both roles focus on GMP compliance, Part Time Gmp Auditors primarily review documentation and processes through audits, whereas Part Time Gmp Inspectors conduct on-site inspections to verify adherence to GMP standards. The roles often overlap but differ in their approach and scope within the industry.

What are some common challenges faced by part-time GMP Auditors, and how can they effectively manage their workload?

Part-time GMP Auditors often face the challenge of balancing audit responsibilities with limited hours, which can make time management and prioritization crucial. They need to efficiently review documentation, conduct site visits, and prepare reports within a condensed schedule. To manage this, it's important to maintain clear communication with the quality assurance team and clients, set realistic goals for each audit, and stay updated on current GMP regulations. Leveraging digital tools and checklists can also help streamline the audit process and ensure thoroughness despite time constraints.

What are part time GMP auditors?

Part time GMP (Good Manufacturing Practice) auditors are professionals who assess manufacturing facilities and processes to ensure they comply with regulatory standards, but do so on a part-time or contract basis. Their main responsibilities include reviewing documentation, inspecting facilities, and identifying areas for improvement to maintain product quality and safety. Part time auditors often work for multiple organizations or as independent consultants, offering flexibility for both the auditor and employer while maintaining high compliance standards.
More about Part Time Gmp Auditor jobs
What are the most commonly searched types of Gmp Auditor jobs? The most popular types of Gmp Auditor jobs are:
What job categories do people searching Part Time Gmp Auditor jobs look for? The top searched job categories for Part Time Gmp Auditor jobs are:
Part Time Gmp Auditor jobs near you
Infographic showing various Part Time Gmp Auditor job openings in the United States as of June 2026, with employment types broken down into 75% Full Time, 24% Part Time, and 1% Contract. Highlights an 88% Physical, 5% Hybrid, and 7% Remote job distribution, with an average salary of $39,947 per year, or $19.2 per hour.

Consultant 1

Eliquent Life Sciences, Inc

Montrose, CA • On-site

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago

Be an early applicant

Job description

ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT is committed to serving clients’ needs with extensive expertise, unwavering integrity, and strategic insight in a manner that supports availability of safe, effective, and high-quality drugs, biologics, and medical devices. For more information, please visit our website at eliquent.com.

We are seeking CSV Consultants at multiple levels (Consultant I, Consultant II, Consultant III) to support validation and compliance activities for computerized systems in a regulated GMP environment. These roles will involve executing validation deliverables, ensuring data integrity, and maintaining inspection readiness across manufacturing, laboratory, and IT systems.

Responsibilities (all levels):

  • Author and/or review CSV documentation, including:
    • Validation Plans, Protocols (IQ/OQ/PQ/FAT/SAT), and Reports
    • User Requirements Specifications (URS), Functional Specifications (FS), and Traceability Matrices
    • Risk assessments and Data Integrity assessments
  • Execute validation testing and document results in compliance with GMP/GLP standards.
  • Support ongoing system lifecycle management: periodic reviews, requalification, and change control.
  • Collaborate with cross-functional teams (Quality, IT, Engineering, Operations, Automation).
  • Provide support during audits and inspections to ensure systems meet regulatory expectations (FDA, EMA, etc.).
  • Ensure compliance with relevant guidelines: GAMP 5, 21 CFR Part 11, EU Annex 11, and company SOPs.

Consultant Levels:

Consultant I (Entry-Level / Junior)

  • Experience: 0–3 years CSV or validation experience in GMP environment
  • Responsibilities: Execute protocols, perform testing, collect evidence, assist with documentation, learn regulatory requirements under supervision.

Consultant II (Mid-Level)

  • Experience: 3–6 years CSV experience, strong working knowledge of FDA/EU regulations, independent execution of validation projects.
  • Responsibilities: Lead small projects or system validations, author protocols and reports, manage deviations, interface with clients and auditors, mentor Consultant I.

Consultant III (Senior-Level)

  • Experience: 6–10+ years CSV or validation leadership experience, expertise in multiple system types (LIMS, MES, SCADA, ERP, Lab/Automation Equipment).
  • Responsibilities: Lead complex CSV programs, oversee multiple system validations, manage validation teams, develop strategies, ensure audit readiness, and advise on compliance.

Qualifications

  • Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related field (required)
  • Knowledge of GMP, GAMP 5, 21 CFR Part 11, EU Annex 11
  • Strong documentation, communication, and organizational skills
  • Ability to work independently and within cross-functional teams
  • Consulting mindset with adaptability to dynamic project needs


BENEFITS:

What We Offer:


Competitive Compensation: Attractive salary and comprehensive benefits package for full-time and part-time employees, including health, dental, vision, and life insurance, a 401(k) plan with employer match, a generous paid time off policy, and additional perks. Compensation is commensurate with professional experience.


Career Development: Opportunities for professional growth and advancement within a supportive and innovative environment.


Work-Life Balance: Flexible work arrangements and a commitment to maintaining a healthy work-life balance.


Eliquent Life Sciences is proud to be an Equal Opportunity Employer, committed to employee diversity.