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Lims Validation Jobs (NOW HIRING)

Catalent, Inc.

LIMS System Administrator

Greenville, NC · On-site

Knowledge of cGMP and other regulatory requirements relative to LIMS systems and software validation experience. * LabVantage experience preferred. * Hands-on experience with GROOVY or Java scripting ...

Syntricate Technologies

Labware LIMS

Skillman, NJ

Hands on Experience in LIMS application development - Interfacing, Upgrade and validation * Experience in Labware Modules like LIMS Stability, EM, Inventory, Storage Location Management, Instrument ...

Technamo

LIMS Administrator

Richmond, VA

The potential candidate will be responsible to upgrade the current version of the LIMS to the latest version and validate the upgrade. The candidate will be working with DGS IT resources and Abbott ...

Weil Group, Inc

Validation Specialist

Juncos, PR

Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are ... Utilize systems such as LIMS , Kneat , and handle Batch Records (BI's) and documentation systems ...

Weil Group, Inc

Validation Specialist

Juncos, PR

Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are ... Utilize systems such as LIMS , Kneat , and handle Batch Records (BI's) and documentation systems ...

Weil Group, Inc.

Validation Specialist

Juncos, PR · On-site

Validation Specialist PQ Focus (E-Beam, Isolators, Filling Equipment) Position Overview We are ... Utilize systems such as LIMS , Kneat , and handle Batch Records (BI's) and documentation systems ...

Technamo LLC

LIMS Administrator

Richmond, VA · On-site

The potential candidate will be responsible to upgrade the current version of the LIMS to the latest version and validate the upgrade. The candidate will be working with DGS IT resources and Abbott ...

Intellectt INC

Validation Engineer

New York, NY · On-site

Perform CSA/CSV for lab systems (LIMS, Empower, Chromeleon) * Develop validation docs: URS, risk assessments, protocols, reports * Ensure compliance with 21 CFR Part 11, GAMP 5, Data Integrity (ALCOA+

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How much do lims validation jobs pay per hour?

As of Jun 7, 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, and why are they important?

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 May 2026, with employment types broken down into 96% Full Time, and 4% Part Time. Highlights an 83% Physical, 5% Hybrid, and 12% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.
LIMS System Administrator

LIMS System Administrator

Catalent, Inc.

Greenville, NC • On-site

Full-time

Life, PTO

Posted 23 days ago

Catalent rating

7.7

Company rating: 7.7 out of 10

Based on 49 frontline employees who took The Breakroom Quiz

45th of 71 rated pharmaceutical

Job description

LIMS System Administrator
Position Summary
  • The shift is Monday - Friday from 8 am - 4:30 pm.
  • This position is 100% on-site at the Greenville site.

The LIMS System Administrator will implement LabVantage Laboratory Information Management System (LIMS) at the Catalent Greenville site. This position is responsible for developing, managing, and implementing the laboratory administration and compliance program for LIMS to ensure compliance with local and global regulatory agency requirements, internal company standards, and current industry practices. Additionally, the LIMS System Administrator will lead cross-functional teams comprised of laboratory, operations, EH&S, and Quality personnel at the Greenville facility and other Catalent sites to expand and improve the use of the LIMS system and to design and implement added-value applications within the LIMS environment.
Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development.
The Role:
  • Perform and support system user access management, including domain user groups, routine access reviews, Windows folder access, and date/time synchronization, as well as resolving end-user LIMS template and data entry issues.
  • Identify operational improvement opportunities which LIMS can provide solutions
  • Lead cross-functional teams to develop site-specific User Requirements in a harmonized format, and collaborate with IT, Quality, CSV, and global system owners to ensure LIMS complies with all applicable GxP, legal, and fiduciary policies and requirements.
  • Define project scope, goals and deliverables that support business goals in collaboration with senior management and stakeholders.
  • Develop and revise site SOPs, including LIMS-specific SOPs in collaboration with the vendor and discipline representatives; author, review, and approve LIMS-related change controls; manage software updates, patches, and routine maintenance upgrades; and author or support validation documentation and system procedures for system qualification of LIMS and its integrations.
  • Support training for end user and handoff for LIMS during new hire orientation (NEO) and implementation.
  • Perform other duties as assigned.

The Candidate:
  • Bachelor's degree in Computer Science, Life Sciences, Engineering, other STEM-related field with at least 5 years of experience in the pharmaceutical industry or relevant laboratory experience in a related industry (OR) Associates degree in Computer Science, Life Sciences, Engineering, other STEM-related field with at least 7 years of experience in the pharmaceutical industry or relevant laboratory experience in a related industry.
  • Experience with LIMS or a Material Management System (e.g., SLIM, IntelliLIMS, LabWare) is required.
  • Knowledge of cGMP and other regulatory requirements relative to LIMS systems and software validation experience.
  • LabVantage experience preferred.
  • Hands-on experience with GROOVY or Java scripting to configure and optimize ELN/LES method workflows, including calculation logic and automated data handling preferred.
  • Ability to work in a manufacturing environment. Ability to stand, walk, and sit for extended periods. Lift up to 25 lbs as needed.

Why You Should Work At Catalent:
  • Spearhead exciting and innovative projects
  • Fast-paced, dynamic environment
  • High visibility to members at all levels of the organization
  • 152 hours of PTO + 8 paid holidays

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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