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Lims Validation Engineer Jobs (NOW HIRING)

supremesoft

CSV Validation QC Engineer

Jersey City, NJ · On-site

Preferred Skills • Experience in Labware, Empower LIMS systems • Experience in validating Lab equipments Job Roles/Responsibilities • Act as Validation and Qualification Lead on a large global ...

Westbourne IT Global Services

... by the validation lead/system manager. * During LIMS upgrades and/or enhancements, perform ... As a Support Engineer, provide support with LIMS system in GxP environment. * Experience in service ...

Ztek Consulting INC

Labware Lims Developer

Albany, NY · On-site

Strong understanding of data governance, version control, and validation protocols. * Familiarity ... LabWare Developer with work experience of at least 7-8 years ABOUT Ztek: Website: www.ztekinc.com ...

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 ...

NeoGenomics

Sr. Software Engineer, LIMS

Fort Myers, FL · Hybrid

$114K - $150K/yr

NeoGenomics is looking for a Senior Software Engineer (LIMS) who wants to learn to continue to ... validate code quality, and ensure adherence to development standards and best practices across ...

MDAEdge

LabWare LIMS-LES Developer

Port Penn, DE · On-site

MDAEdge is seeking a skilled LabWare LIMS-LES Developer to support and enhance their Laboratory ... Perform system testing, validation, and documentation according to defined protocols. • ...

NeoGenomics

Sr. Software Engineer, LIMS

Ramsey, NJ · Hybrid

$121K - $160K/yr

NeoGenomics is looking for a Senior Software Engineer (LIMS) who wants to learn to continue to ... validate code quality, and ensure adherence to development standards and best practices across ...

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 ... Collaborate with Engineering, Operations, and Quality to maintain validated and secure environments.

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How much do lims validation engineer jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for lims validation engineer 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.

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Infographic showing various Lims Validation Engineer job openings in the United States as of September 2026, with employment types broken down into 80% Full Time, 5% Part Time, and 15% Contract. Highlights an 90% In-person, and 10% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

6493 - Lab CSV Engineer / Senior CSV Engineer

Indianapolis, IN • On-site

Verista, Inc.
Pharmaceutical and Medicine Manufacturing • 201 - 500 employees
Learn more about Verista, Inc.external

$99K - $137K/yr

Full-time

Posted 16 days ago

Job description

Senior Validation Engineer Responsibilities:

  • Lead and execute computer system validation and equipment qualification activities for laboratory equipment integrated with LabVantage LIMS in a GxP-regulated environment
  • Qualify and validate laboratory instruments and systems, with a primary focus on Climet environmental monitoring instruments and similar laboratory equipment that interface with LabVantage
  • Execute vendor-provided qualification documentation and protocols, including SAT, IQ, OQ, and related testing, ensuring activities are performed in accordance with approved procedures and protocols
  • Support the execution and documentation of qualification activities for laboratory instruments, primarily using existing approved protocols and documentation with minor updates to reflect equipment-specific differences
  • Leverage existing approved validation and qualification documentation to efficiently develop or update URS, risk assessments, IQ/OQ documentation, test scripts, traceability, and validation summary documentation for equipment that is substantially equivalent to existing qualified units
  • Evaluate existing equipment qualification and validation packages to identify required updates based on instrument configuration, LIMS integration, software, hardware, or other equipment-specific differences
  • Perform and document testing of LIMS interfaces and data flows associated with laboratory instruments, ensuring accurate, complete, and reliable transfer of data between equipment and LabVantage
  • Review vendor documentation and protocols for completeness and applicability and identify any gaps or deviations requiring resolution prior to or during execution
  • Execute validation and qualification activities in accordance with GxP, data integrity, 21 CFR Part 11, company validation procedures, and applicable CSV/CSA principles
  • Document test results, deviations, discrepancies, and exceptions and support resolution through appropriate investigation, change control, and CAPA processes
  • Collaborate with Laboratory, Quality, IT, Validation, equipment vendors, and system owners to coordinate qualification activities and resolve technical or documentation issues
  • Support validation documentation closeout, ensuring qualification packages are complete, accurate, traceable, and audit-ready
  • Provide technical support for the laboratory equipment and LabVantage environment following qualification, including troubleshooting and assessment of changes impacting the validated state

Job Requirements:

  • Bachelor's degree in Engineering, Computer Science, Life Sciences, Information Systems, or related technical discipline
  • 5+ years of CSV, equipment qualification, or validation experience in a regulated life sciences environment
  • 2-3+ years of experience qualifying laboratory equipment integrated with a LIMS, with hands-on LabVantage LIMS experience strongly preferred
  • Demonstrated experience executing vendor-provided qualification protocols, including SAT and IQ/OQ, and accurately documenting test results, deviations, and exceptions
  • Experience developing, reviewing, and executing validation and qualification documentation, including URS, risk assessments, IQ/OQ, test scripts, traceability, deviations, and validation summary reports
  • Ability to leverage existing approved qualification and validation packages and efficiently adapt documentation for equivalent or similar laboratory equipment with minimal configuration differences
  • Strong understanding of GxP, CSV/CSA, data integrity, 21 CFR Part 11, change control, and validation lifecycle requirements, including testing of LIMS interfaces and data flows
  • Strong attention to detail, organization, troubleshooting, and communication skills, with the ability to manage a high-volume validation backlog and collaborate effectively with Laboratory, Quality, IT, Validation, and equipment vendors

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