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Lims Validation Jobs (NOW HIRING)

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 ...

Clarkston Consulting

LIMS Consultant

Philadelphia, PA · On-site +1

Come join us as a LIMS Consultant, and in this role, you will deliver creative business solutions ... Design, configure, and validate assay workflows within, ensuring alignment with scientific ...

Clarkston Consulting

LIMS Consultant

Atlanta, GA · On-site +1

Come join us as a LIMS Consultant, and in this role, you will deliver creative business solutions ... Design, configure, and validate assay workflows within, ensuring alignment with scientific ...

Infogene

Lims H/F

Participation in implementation phases, data migration, and validation (CSV) * Integration of LIMS with other systems (ERP, MES, laboratory instruments, middleware...) * Support to users, training ...

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 ...

Clarkston Consulting

LIMS Consultant

Dallas, TX · On-site +1

Come join us as a LIMS Consultant, and in this role, you will deliver creative business solutions ... Design, configure, and validate assay workflows within, ensuring alignment with scientific ...

AMRI

Senior Specialist LIMS

Rensselaer, NY · On-site

$81K - $112K/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 ...

Curia, Inc.

Senior Specialist LIMS

Rensselaer, NY · On-site

$81K - $112K/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 ...

Clarkston Consulting

LIMS Consultant

Detroit, MI · On-site +1

Come join us as a LIMS Consultant, and in this role, you will deliver creative business solutions ... Design, configure, and validate assay workflows within, ensuring alignment with scientific ...

Veracyte

Manager, LIMS

San Diego, CA · On-site

$169K - $181K/yr

As the Manager, LIMS, you will lead the administration, enhancement, and operational excellence of ... Oversee system configuration, validation, implementation, release management, and ongoing ...

Semaphore Solutions

LIMS Consultant

Boston, MA · Remote

This role spans consultation, requirements gathering, documentation, LIMS configuration, validation testing, support ticket resolution, and light project management. Youll collaborate cross ...

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 ...

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All JobsLims Validation Jobs

LIMS Validation information

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$22

$51

$78

How much do lims validation jobs pay per hour?

As of Aug 12, 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?

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 August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 3% Part Time, 1% Temporary, and 7% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Labware LIMS Specialist

Staffingine LLC

Summit, NJ • On-site

Contractor

Re-posted 4 days ago

Job description

Job Title: Labware LIMS Specialist
Job Location: Summit, NJ
Job Type: Contract

Job Description:

  • Strong Concepts of LIMS and LabWare V6 V7 V8
  • Detailed knowledge on Labware LIMS Architecture Labware Database Structures SAP Crystal Reports Oracle PLSQL
  • 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 Location Management Instrument Interfaces Lot Sample Management for Clinical Trial Manufacturing Domain
  • Hands on experience on requirement gathering and configuration and development of Laboratory Information Management SystemLIMS eg LabWare preferably V5V6V7 expertise
  • Experience in Labware Modules like LIMS Stability EM Inventory Storage Location Management Instrument Interfaces Lot Sample Management for Clinical Trial Manufacturing Domain
  • Ability to Solve all Technical Issues in Labware LIMS including Interfaces to ERP Label Printing Software MDM and all modules
  • Carried out relevant support activities like ensuring 24X7 application availability Process Improvement Automation Impact analysis and replication of application issues et al
  • Have hands on experience in SDLC and Agile model delivery in ITIL and ITSM process integrations
  • Knowledge of Pharma domain
  • Conduct GxP Analysis Gap or Risk Assessment
  • Experience with risk based approaches for IT Application development
  • Ability to work independently manage multiple priorities and work in an unstructured environment
  • Excellent oral and written communication skills
  • Labware Certification
  • Configure objects for Labs as and when required or requested Trouble shooting problems Root cause analysis Validation and execution of LIMS projects
  • Should have good knowledge of LIMS system architecture and functionality
  • Should have handled Administrative responsibilities for Lab system applications

Mandatory Skills : Labvantage,LabWare,SampleManager,StarLIMS,Empower,Lab Management Systems,Caliber LIMS,AR_VR_MR