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Part Time Lims Consultant information

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$10

$41

$87

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

As of Jun 24, 2026, the average hourly pay for part time lims consultant in the United States is $41.55, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $49.52 per hour, depending on experience, location, and employer.

What is the difference between Part Time Lims Consultant vs Part Time Laboratory Technician?

AspectPart Time Lims ConsultantPart Time Laboratory Technician
CredentialsTypically requires a degree in life sciences or related field, plus LIMS certificationUsually requires a high school diploma or associate degree, with laboratory training
Work EnvironmentConsulting firms, laboratories, or biotech companies, focusing on system implementation and supportLaboratories, hospitals, or research facilities, performing sample testing and data entry
Employer & Industry UsageUsed by biotech, pharmaceutical, and clinical labs for system managementCommon in healthcare, research, and environmental testing labs

The main difference is that a Part Time Lims Consultant focuses on implementing and supporting Laboratory Information Management Systems, requiring specialized knowledge and certifications. In contrast, a Part Time Laboratory Technician performs hands-on testing and data entry within laboratory settings. Both roles are essential but serve different functions within the laboratory industry.

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

To thrive as a Part Time LIMS Consultant, you need expertise in laboratory information management systems (LIMS), a background in laboratory science or IT, and experience with data integration. Familiarity with major LIMS platforms (such as LabWare, STARLIMS, or Thermo Fisher), SQL databases, workflow configuration, and relevant certifications like CLIMB or vendor-specific credentials is often required. Strong analytical thinking, communication, and problem-solving skills help consultants effectively liaise between stakeholders and ensure optimal system performance. These skills and qualifications are crucial for successfully implementing, customizing, and supporting LIMS solutions that meet diverse laboratory needs.

What is a Part Time LIMS Consultant?

A Part Time LIMS Consultant is a professional who specializes in Laboratory Information Management Systems (LIMS) and works on a part-time basis. They assist laboratories in selecting, implementing, configuring, and maintaining LIMS software to streamline data management and laboratory workflows. Part time consultants may work remotely or onsite, providing expertise on system integration, user training, and troubleshooting. Their flexible schedule allows laboratories to access LIMS expertise without the commitment of a full-time hire.

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

Part-time LIMS consultants often juggle several projects for different clients, which can present challenges such as managing varying project timelines, adapting to different laboratory workflows, and ensuring clear communication despite part-time availability. It’s important to set realistic expectations with each client regarding response times and deliverables. Staying organized and maintaining strong documentation practices can help manage priorities and provide consistent, high-quality support across multiple implementations.
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Part Time Lims Consultant jobs near you
Infographic showing various Part Time Lims Consultant job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $86,430 per year, or $41.6 per hour.

Consultant 1

Eliquent Life Sciences, Inc

Montrose, CA • On-site

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 hours 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.