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Lims Validation Jobs (NOW HIRING)

Staffingine LLC

LIMS Specialist

Raritan, NJ · Remote

Hands on Experience in LIMS application development LIMS basic Language Subroutines Interfacing Upgrade and validation * Experience in Labware Modules like LIMS Stability EM Inventory Storage ...

Staffingine LLC

Labware LIMS Specialist

Summit, NJ · On-site

Hands on Experience in LIMS application development LIMS basic Language Subroutines Interfacing Upgrade and validation * Experience in Labware Modules like LIMS Stability EM Inventory Storage ...

Syntricate Technologies

Labware LIMS

Skillman, NJ · On-site

Hands on Experience in LIMS application development - Interfacing, Upgrade and validation * Experience in Labware Modules like LIMS Stability, EM, Inventory, Storage Location Management, Instrument ...

AMRI

Senior Specialist LIMS

Rensselaer, NY

$117K - $145K/yr

Senior Specialist LIMS in Rensselaer, NY Build your future at Curia, where our work has the power ... Validation & Compliance:Execute validation activities, ensuring compliance with GxP, data integrity ...

Viatris

Associate - LIMS

Morgantown, WV · On-site

... validation samples. * Assist with creation of LIMS Product Specifications, Item Codes, and related LIMS components for all new products. * Assist with revising LIMS Product Specifications, Item Codes ...

MDAEdge

LabWare LIMS-LES Developer

Raleigh, NC · On-site

... validation, and documentation according to defined protocols. • Participate in upgrades, patches, and performance optimization of the LabWare system. Qualifications : Required : • Proven ...

TMS

LIMS Business Analyst

Richmond, VA · On-site

... validation,test case development, and quality assurance activities · Creating documentation for business requirements, functional specifications, and solution designs · Eliciting and documenting ...

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Lims Validation information

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How much do lims validation jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for lims validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a LIMS Validation Specialist, and why are they important?

To excel as a LIMS Validation Specialist, you need a strong background in laboratory processes, software validation, and knowledge of regulatory requirements, often supported by a degree in life sciences or IT. Familiarity with Laboratory Information Management Systems (LIMS), validation protocols (IQ/OQ/PQ), and tools like SQL or scripting languages is typically required. Attention to detail, problem-solving ability, and effective communication are crucial soft skills for ensuring compliance and collaborating with cross-functional teams. These competencies are vital to guarantee data integrity, regulatory compliance, and the successful implementation of LIMS in laboratory environments.

What is LIMS validation?

LIMS validation is the process of ensuring that a Laboratory Information Management System (LIMS) meets regulatory requirements and performs as intended. This involves documented testing of the software to confirm its accuracy, reliability, and consistent intended performance in a specific laboratory environment. Validating a LIMS is crucial for compliance with standards such as FDA 21 CFR Part 11 or ISO 17025, and helps ensure data integrity and traceability. The process typically includes risk assessment, protocol development, execution, and documentation of results. Proper validation reduces the risk of errors and supports laboratory operations and audits.

What is the difference between Lims Validation vs Lims Analyst?

AspectLims ValidationLims Analyst
CertificationsGxP, 21 CFR Part 11 compliance, validation certificationsGxP, 21 CFR Part 11 familiarity, relevant certifications
Work EnvironmentQuality assurance, validation teams, regulated labsLaboratories, data analysis, system monitoring
Industry UsagePharmaceutical, biotech, clinical labsLaboratory operations, data management

While Lims Validation focuses on ensuring Laboratory Information Management Systems meet regulatory standards through validation processes, Lims Analysts primarily handle data analysis, system monitoring, and supporting laboratory operations. Both roles require familiarity with GxP regulations, but Lims Validation is more specialized in validation procedures, whereas Lims Analysts focus on data integrity and system performance.

What are some common challenges faced when validating a Laboratory Information Management System (LIMS), and how can they be addressed?

One common challenge in LIMS validation is ensuring the system meets both regulatory compliance and the specific needs of the laboratory. This often requires close collaboration with IT, QA, and lab staff to gather and translate user requirements into testable validation protocols. Another challenge is managing software updates or customizations without disrupting validated processes. Staying organized with thorough documentation and leveraging validation templates can help streamline the process and ensure ongoing compliance. Open communication and regular training within the validation team are also key to addressing unexpected issues efficiently.
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Lims Validation jobs near you
Infographic showing various Lims Validation job openings in the United States as of July 2026, with employment types broken down into 3% Internship, 87% Full Time, 1% Part Time, 1% Temporary, 7% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.
Labware LIMS Validation Specialist

Labware LIMS Validation Specialist

Intellectt INC

Thousand Oaks, CA • On-site

Contractor

Posted 3 days ago

Job description

Job Title: Lab Ware LIMS Validation Specialist
Location: Thousand Oaks, CA -Hybrid
Duration: 12+ Months Contract

Job Summary:
Seeking an experienced Lab Ware LIMS Validation Specialist to support validation activities for laboratory systems in a regulated pharmaceutical environment. The role focuses on Computer System Validation, Lab Ware LIMS compliance, and ensuring alignment with GMP, GxP, FDA, 21 CFR Part 11, GAMP 5, and internal quality standards.

Key Responsibilities:

  • Execute validation activities for Lab Ware LIMS in compliance with GxP, FDA, and industry regulations.
  • Author, review, and execute validation documents including URS, Risk Assessments, IQ, OQ, PQ, Traceability Matrix, and Validation Summary Reports.
  • Collaborate with business, quality, and IT teams to gather and document system requirements.
  • Support change controls, deviations, CAPAs, and periodic reviews related to Lab Ware LIMS.
  • Ensure compliance with 21 CFR Part 11, GAMP 5, and internal quality standards.
  • Participate in system upgrades, enhancements, and remediation activities.
  • Provide validation support during audits and inspections.

Skills Required:

  • 5+ years of Computer System Validation experience in pharmaceutical or biotechnology environments.
  • Hands-on experience validating Lab Ware LIMS applications.
  • Strong knowledge of GxP, GMP, FDA regulations, 21 CFR Part 11, and GAMP 5.
  • Experience preparing and executing validation documentation such as URS, IQ, OQ, PQ, Risk Assessments, Traceability Matrix, and Validation Summary Reports.
  • Strong understanding of change controls, deviations, CAPAs, and periodic review processes.
 

For more information, please reach out at 732-719-4936 or share your updated resume with padma.priya@intellectt.com.