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Lims Csv Jobs (NOW HIRING)

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 ...

PACIV

IT / CSV Specialist

San Juan, PR · On-site

... IT / CSV Specialist to provide technical support for laboratory applications, systems ... Provide IT support for laboratory applications such as Empower, SmartLab, and Darwin LIMS.

FUJIFILM Holdings America Corporation

Position Overview The QC LIMS Developer designs, configures, validates, and supports Laboratory ... Author and execute CSV deliverables: URS, FRS, HDS, configuration specs, risk assessments, test ...

Fujifilm

QC LIMS Developer

Durham, NC · On-site

Author and execute CSV deliverables: URS, FRS, HDS, configuration specs, risk assessments, test ... LabWare LIMS Basic or LabVantage Java/Groovy; .NET/Java/Python for integrations; XML/JSON.

Fujifilm

QC LIMS Developer

Research Triangle Park, NC · On-site

The QC LIMS Developer designs, configures, validates, and supports Laboratory Information ... Author and execute CSV deliverables: URS, FRS, HDS, configuration specs, risk assessments, test ...

PM Group

CSV Engineer I

Indianapolis, IN · On-site

$68K - $88K/yr

Overview The CSV Engineer I position is an exciting opportunity to join PM Group's quickly growing ... Support validation activities for laboratory systems such as LIMS, CDS, ELN, SDMS, standalone ...

MDAEdge

LabWare LIMS-LES Developer

Raleigh, NC · On-site

MDAEdge is looking for a skilled LabWare LIMS-LES Developer to support and enhance their LabWare ... CSV), change control, and regulatory requirements (FDA 21 CFR Part 11, GxP). • Good analytical ...

Nanda Technologies

CSV Engineer

Costa Mesa, CA · On-site

$55 - $60/hr

CSV Engineer Costa Mesa, CA or Seattle, WA(On-site) Visa: USC, GC & H4 EAD Key Responsibilities ... Familiarity with LIMS, MES, SCADA, or laboratory instrumentation. * Prior exposure to audits or ...

InterSources Inc

Labware LIMS Validation Engineer

They are seeking a Labware LIMS Validation Engineer to provide expertise in Labware Meta Data and ... Labware Version8. • Labware CSV • Meta Data Storage Location • Meta Storage Limit ...

PM Group

CSV Engineer I

Indianapolis, IN · On-site

$68K - $88K/yr

Overview The CSV Engineer I position is an exciting opportunity to join PM Group's quickly growing ... Support validation activities for laboratory systems such as LIMS, CDS, ELN, SDMS, standalone ...

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 ... CSV), change control, and regulatory requirements (FDA 21 CFR Part 11, GxP). • Good analytical ...

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How much do lims csv jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for lims csv in the United States is $38.08, according to ZipRecruiter salary data. Most workers in this role earn between $24.04 and $50.48 per hour, depending on experience, location, and employer.

What is a LIMS CSV?

LIMS CSV refers to professionals who specialize in Computer System Validation (CSV) for Laboratory Information Management Systems (LIMS). Their main responsibility is to ensure that LIMS software complies with regulatory standards and functions correctly in laboratory environments. This involves planning, writing, and executing validation protocols, documenting processes, and ensuring data integrity. LIMS CSV specialists often work closely with IT, QA, and laboratory staff to implement, test, and maintain validated systems. Their work is critical for organizations in regulated industries, such as pharmaceuticals and biotechnology, where compliance with FDA, GxP, and other standards is required.

What skills and qualifications are needed to thrive as a LIMS CSV specialist?

To thrive as a LIMS CSV Specialist, you need a strong background in laboratory information management systems, computer system validation principles, and relevant regulatory standards such as GxP or 21 CFR Part 11, typically supported by a degree in life sciences, IT, or a related field. Familiarity with validation protocols, risk assessment tools, and documentation systems like Veeva Vault or MasterControl is highly valuable. Exceptional attention to detail, analytical thinking, and effective communication are essential soft skills in this role. These competencies ensure validated, compliant, and reliable laboratory systems, which are critical for quality assurance and meeting regulatory requirements in scientific environments.

What are common challenges faced when validating data in a LIMS CSV role, and how can they be addressed?

Professionals working in a LIMS CSV (Laboratory Information Management System Computer System Validation) role often encounter challenges such as ensuring data integrity, managing frequent software updates, and meeting strict regulatory requirements. Addressing these challenges involves staying updated with evolving compliance guidelines, developing robust validation protocols, and collaborating closely with lab personnel and IT teams. Clear documentation and regular training are essential to maintain data accuracy and ensure successful audits.

What other helpful pages are available for Lims Csv?

Other pages related to Lims Csv:

Infographic showing various Lims Csv job openings in the United States as of September 2026, with employment types broken down into 89% Full Time, 2% Part Time, 1% Temporary, 7% Contract, and 1% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $79,207 per year, or $38.1 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 13 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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