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Lims Csv Jobs (NOW HIRING)

Astrix Inc

CSV Specialist

Lexington, MA · On-site

$45 - $52/hr

Hyrbrid - 3 days a week in person (Lexington, MA) Pay: $45-52/hr 6month contract The CSV Engineer ... Familiarity with MODA, LabWare, or other QC/LIMS platforms preferred. * Proficient in Microsoft ...

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 ... Collaborate with scientists, QA/CSV teams, and IT to gather requirements, design technical ...

AMRI

Senior Specialist LIMS

Rensselaer, NY

$81K - $112K/yr

Senior Specialist LIMS in Rensselaer, NY with relocation assistance Build your future at Curia ... Execute validation activities, ensuring compliance with GxP, data integrity, and CSV requirements.

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 ... Execute validation activities, ensuring compliance with GxP, data integrity, and CSV requirements.

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 ... Collaborate with scientists, QA/CSV teams, and IT to gather requirements, design technical ...

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 ... Collaborate with scientists, QA/CSV teams, and IT to gather requirements, design technical ...

PM Group

CSV Engineer III

Indianapolis, IN

$68K - $88K/yr

Overview The CSV Engineer III position is an exciting opportunity to join PM Group's quickly ... Support validation of laboratory systems such as LIMS, chromatography data systems, laboratory ...

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 ... Collaborate with scientists, QA/CSV teams, and IT to gather requirements, design technical ...

ClifyX

QC and LIMS

Springfield, NJ · On-site

Lead or assist in Computer System Validation (CSV), equipment qualification, and periodic review ... Proven experience with GMP regulations, QC software (e.g., LIMS, CDS), and laboratory instruments.

PM Group

CSV Engineer III

Indianapolis, IN · On-site

$68K - $88K/yr

Overview The CSV Engineer III position is an exciting opportunity to join PM Group's quickly ... Support validation of laboratory systems such as LIMS, chromatography data systems, laboratory ...

Zifo

LIMS Analyst (LabVantage)

Boston, MA · On-site

System validation and CSV documentation experience * Exposure to LIMS integrations or configuration scripting * Consulting or client-facing experience * Experience supporting instrument or inventory ...

Zifo

LIMS Analyst (LabVantage)

Boston, MA · On-site

System validation and CSV documentation experience * Exposure to LIMS integrations or configuration scripting * Consulting or clientfacing experience * Experience supporting instrument or inventory ...

ALLIANCE BIOTECH SOLUTIONS LLC

CSV Engineer

Raleigh, NC · On-site

... LIMS, MES, ERP, PI Historian, and related GxP systems. Verify data integrity, security, audit trail ... CSV, CSA, database validation, and data integrity best practices. Experience & Skills Bachelor ...

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Lims Csv information

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How much do lims csv jobs pay per hour?

As of Sep 10, 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.

CSV Specialist

Lexington, MA • On-site

Astrix Inc
Recruiting and Staffing Services • 1 - 5K employees
Learn more about Astrix Incexternal

$45 - $52/hr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Pay Rate Low: 45.00 | Pay Rate High: 52.00
**We cannot support C2C or provide sponsorship for this opportunity**
Hyrbrid - 3 days a week in person (Lexington, MA)
Pay: $45-52/hr
6month contract
The CSV Engineer is responsible for validating GxP computer systems and ensuring compliance with global procedures, data integrity standards, and applicable regulations. The role partners closely with Quality Systems, QC, Project Management, and technical SMEs to deliver high-quality validation documentation and execution.
Responsibilities
  • Lead full validation lifecycle per GAMP 5 and cGxP requirements.
  • Develop and maintain Validation Plans, URS, OQ/PQ protocols, traceability matrices, and summary reports.
  • Author and execute test scripts in HP ALM with complete requirement linkage.
  • Validate system configurations, data flows, and electronic records for compliance with 21 CFR Part 11.
  • Perform regression testing to ensure changes do not impact existing functionality or data integrity.
  • Manage defects, deviations, and root cause documentation within electronic systems.
  • Collaborate with business and system SMEs to translate requirements into validated system states.
  • Maintain strong communication and cross-functional coordination.

Qualifications
  • Bachelor's degree in engineering or life sciences; equivalent experience considered.
  • Minimum 5 years in pharmaceutical or biopharmaceutical CSV.
  • Strong understanding of cGxP, GAMP5, S88, 21 CFR Part 11.
  • Experience with TrackWise, Veeva, Kneat, ALM, or similar documentation systems.
  • Familiarity with MODA, LabWare, or other QC/LIMS platforms preferred.
  • Proficient in Microsoft Teams and electronic collaboration tools.

Apply