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Part Time Gmp Consultant 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 ...

Certified Group

Part-time Courier

Dallas, TX · On-site

$15.50 - $19.75/hr

EAS Consulting Group - A regulatory consulting firm offering expert guidance, training, and ... GMP programs. Job Summary The Courier I is responsible for the safe, efficient, and timely pick-up ...

Bechtel

Senior Counsel

Houston, TX

$133K - $181K/yr

Telework Type: Part-Time Telework * Work Location: Houston, TX, Reston, VA Extraordinary teams ... consultation with functional or project leadership. Major Responsibilities: * Work closely with ...

Kedrion S.p.A.

Medical Director

Phoenix, AZ · On-site

This is a part-time role that as a licensed M.D. or D.O. would dedicate about 10 hours a week What ... Provide consultation on donor medical emergencies and suitability, including on-call availability.

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Part Time Gmp Consultant information

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$10

$49

$118

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

As of Jul 20, 2026, the average hourly pay for part time gmp consultant in the United States is $49.72, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $62.50 per hour, depending on experience, location, and employer.

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

AspectPart Time Gmp ConsultantPart Time Gmp Auditor
CredentialsGMP certification, industry experienceGMP certification, auditing training
Work EnvironmentAdvisory, consulting projectsInspection, compliance review
Employer & IndustryPharmaceutical companies, consulting firmsRegulatory agencies, pharma companies

Part Time Gmp Consultants primarily provide expert advice to ensure compliance and optimize GMP processes, while Part Time Gmp Auditors focus on inspecting and verifying adherence to GMP standards. Both roles require GMP certification and are common in pharmaceutical industries, but their core functions differ: consulting versus auditing.

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

To thrive as a Part Time GMP Consultant, you need in-depth knowledge of Good Manufacturing Practices, regulatory compliance, and quality assurance, typically supported by a science degree and industry experience. Familiarity with quality management systems (QMS), audit tools, and relevant certifications such as GMP or ISO are highly valuable. Excellent communication, analytical thinking, and the ability to provide clear guidance make someone stand out in this consulting role. These skills ensure clients remain compliant, minimize risk, and maintain high standards in regulated manufacturing environments.

What is a Part Time GMP Consultant?

A Part Time GMP Consultant is a professional who provides expert guidance on Good Manufacturing Practices (GMP) to organizations in the pharmaceutical, biotechnology, or food industries, but works on a part-time or contract basis. Their responsibilities may include auditing facilities, developing compliance strategies, training staff, and ensuring that processes meet regulatory standards. Working part time allows companies to access specialized expertise as needed without hiring a full-time employee.

What are some common challenges faced by part-time GMP consultants when working with multiple clients?

Part-time GMP consultants often juggle projects for several clients, which can create challenges in managing differing expectations, schedules, and documentation standards. Consultants must quickly adapt to each client's specific processes and maintain clear communication to ensure compliance with Good Manufacturing Practices. Time management and prioritization are essential, as consultants are expected to deliver high-quality advice and audits efficiently within limited hours. Building strong relationships with internal teams also helps streamline collaboration and problem-solving.
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Part Time Gmp Consultant jobs near you
Infographic showing various Part Time Gmp Consultant job openings in the United States as of July 2026, with employment types broken down into 2% Locum Tenens, 87% Full Time, 7% Part Time, and 4% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $103,425 per year, or $49.7 per hour.

Consultant 1

Eliquent Life Sciences, Inc

Montrose, CA • On-site

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 26 days ago

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.