ZipRecruiter

Log In

1

Lims Validation Jobs (NOW HIRING)

Zifo

LIMS Analyst (LabVantage)

Boston, MA · On-site

This role is focused on delivering sample-centric LIMS solutions , supporting the full sample ... Develop and execute system testing and validation deliverables (IQ/OQ/PQ, test scripts ...

MDAEdge

LabWare LIMS-LES Developer

Port Penn, DE · On-site

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

Fujifilm

QC LIMS Developer

Durham, NC · On-site

Position Overview The QC LIMS Developer designs, configures, validates, and supports Laboratory Information Management System (LIMS) capabilities for Quality Control laboratories. This role builds ...

Weil Group, Inc

Sample & Management LIMS Coordinator

Juncos, PR · On-site

$17.75 - $24.25/hr

Collaborate with QC, Manufacturing, Quality, Validation, IT, and other cross-functional groups to resolve sample or system-related issues. * Ensure sample management and LIMS activities are performed ...

FUJIFILM Holdings America Corporation

Position Overview The QC LIMS Developer designs, configures, validates, and supports Laboratory Information Management System (LIMS) capabilities for Quality Control laboratories. This role builds ...

Pinnaql

CQV Sample Management / LIMS Coordinator

Juncos, PR · On-site

$17.75 - $24/hr

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... CQV Sample Management / LIMS Coordinator Job Summary: We are seeking an experienced CQV Sample ...

Fujifilm

QC LIMS Developer

Research Triangle Park, NC · On-site

The QC LIMS Developer designs, configures, validates, and supports Laboratory Information Management System (LIMS) capabilities for Quality Control laboratories. This role builds compliant digital ...

Fujifilm

QC LIMS Developer

Research Triangle Park, NC · On-site

Position Overview The QC LIMS Developer designs, configures, validates, and supports Laboratory Information Management System (LIMS) capabilities for Quality Control laboratories. This role builds ...

previous page

Showing results 41-60

All JobsTechnology JobsSoftware JobsSoftware Quality Engineer JobsLims Validation Jobs

Lims Validation information

See salary details

$22

$51

$78

How much do lims validation jobs pay per hour?

As of Sep 13, 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 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 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 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.

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.

More about Lims Validation jobs

What cities are hiring for Lims Validation jobs?

Cities with the most Lims Validation job openings:

What states have the most Lims Validation jobs?

States with the most job openings for Lims Validation jobs include:

What job categories do people searching Lims Validation jobs look for?

The top searched job categories for Lims Validation jobs are:

What other helpful pages are available for Lims Validation?

Other pages related to Lims Validation:

Lims Validation jobs near you
Infographic showing various Lims Validation job openings in the United States as of September 2026, with employment types broken down into 91% Full Time, 4% Part Time, 1% Temporary, and 4% Contract. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Computer System Validation (CSV) Consultants

Piscataway, NJ • On-site

Resourcesys
11 - 50 employees
Learn more about Resourcesysexternal

Other

Posted 18 days ago

Job description


Job Title:- Computer System Validation (CSV) Consultants
Location:- Piscataway, NJ/Chicago, IL (Onsite)
Duration:- Contract to hire
Job Description

Responsibilities

  • Plan, author, execute, and maintain CSV documentation including Validation Plans (VP), User Requirements Specifications (URS), Functional Specifications (FS), Design Specifications (DS), IQ/OQ/PQ protocols, Traceability Matrices, and Validation Summary Reports.
  • Perform CSV activities for laboratory instruments, engineering/manufacturing equipment, and enterprise applications.
  • Validate systems including LIMS, SAP, CMMS/calibration platforms, and other GxP-regulated applications.
  • Partner with system owners, Quality, IT, Laboratory, and Manufacturing teams to maintain systems in a validated state through change control and periodic reviews.
  • Conduct risk assessments and data-integrity assessments aligned with ALCOA+ principles.
  • Support audits, inspections, CAPAs, deviations, and remediation activitiesrelated to computerized systems.
  • Apply GAMP 5 and risk-based validation principles throughout the system lifecycle.
  • Support validation activities involvingCaliber LIMS, SAP QM/MM/PP, BMRAM or comparable CMMS/calibration systems where applicable.

Required Qualifications

  • 5+ years of Computer System Validation experience within a GxP-regulated environment.
  • Strong, demonstrable CSV experience specifically within Biotechnology/Biotech environments REQUIRED.
  • Hands-on experience authoring and executing IQ/OQ/PQ protocols.
  • Strong working knowledge of 21 CFR Part 11, EU Annex 11, GxP, GAMP 5, and risk-based validation.
  • Experience validating at least two of the following:
    • Laboratory instruments
    • Manufacturing/engineering equipment
    • LIMS
    • SAP
    • CMMS/calibration systems
  • Experience working cross-functionally withQuality, IT, Laboratory, Manufacturing, and technical SMEs.
  • Bachelor's degree in Life Sciences, Engineering, IT, or equivalent relevant life-sciences laboratory experience.
  • Ability and willingness to work onsite 5 days per week.
  • Candidates must be interested and eligible for a contract-to-hire opportunity.

Apply