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Lims Professional Jobs in Virginia (NOW HIRING)

Winaxis

Network Engineering

Richmond, VA · On-site

$55/hr

... with a professional and friendly attitude. - Contribute to the modernization and integration of lab equipment with the CoreOne LIMS system. - Travel 3-4 times per week, including at least one ...

advansix

Quality Manager

Chester, VA · On-site

$118K - $178K/yr

Professional certifications such as CQE, Six Sigma Green/Black Belt. * Experience with LIMS and statistical software (e.g., Minitab, JMP). The expected base pay for this position is $118,800 - $178 ...

advansix

Quality Manager

Chester, VA · On-site

$118K - $178K/yr

Professional certifications such as CQE, Six Sigma Green/Black Belt. * Experience with LIMS and statistical software (e.g., Minitab, JMP). The expected base pay for this position is $118,800 - $178 ...

Instant Serve LLC

Oracle DBA

Richmond, VA · On-site

$50.25 - $68.25/hr

Oracle Certified Professional (OCP) certification preferred. Familiarity with SQL Server Support ... LIMS Database. The on-call rotation begins on Saturday and ends the following Friday. The agency ...

Onterris

QA Associate - Laboratories

Richmond, VA

$20 - $23/hr

Our scientists, engineers, field teams,consultantsand professionals collaborate across disciplines ... Experience with LIMS. * Proficiency using and data visualization tools for reports and graphs.

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Lims Professional information

What is the difference between Lims Professional vs Laboratory Technician?

AspectLims ProfessionalLaboratory Technician
CredentialsTypically requires a degree in life sciences or related field, with certifications in laboratory information management systems (LIMS)Usually requires a high school diploma or associate degree, with some technical training
Work EnvironmentWorks primarily with LIMS software, data management, and quality control in labsPerforms sample testing, data recording, and basic lab procedures
Industry UsageCommon in biotech, pharmaceutical, and clinical labs for data managementFound in similar settings, focusing on sample processing and testing

The main difference is that Lims Professionals focus on managing laboratory data and systems, requiring specialized software knowledge, while Laboratory Technicians perform hands-on testing and sample analysis. Both roles are essential in laboratory operations but differ in responsibilities and skill requirements.

What is a LIMS professional job description?

A LIMS (Laboratory Information Management System) professional is responsible for implementing, maintaining, and optimizing laboratory software systems that manage data, samples, and workflows. They often collaborate with lab staff to ensure system accuracy, troubleshoot issues, and may require knowledge of database management, programming, and industry regulations. Certification and technical skills are typically important for this role.

What are the most commonly searched types of Lims jobs in Virginia?

The most popular types of Lims jobs in Virginia are:

What are popular job titles related to Lims Professional jobs in Virginia?

For Lims Professional jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Lims Professional jobs in Virginia look for?

The top searched job categories for Lims Professional jobs in Virginia are:

What cities in Virginia are hiring for Lims Professional jobs?

Cities in Virginia with the most Lims Professional job openings:

Lims Professional jobs near you

Reagent and Standards Administrator

FAREVA

Richmond, VA

Full-time

Posted 5 days ago

Key responsibilities

  • Manage ordering, inventory, processing, and reconciliation of laboratory reference standards and reagents.

  • Oversee full sample life cycle, including collection, logging, labeling, delivery, and disposal of QC samples.

  • Perform physical and analytical testing on production samples, record results, and assist in investigations.

Job description

Job Title: Reagent and Standards Administrator

Company: Fareva Richmond

Reports To: QC Supervisor or QC Manager

Date Updated: July 2026

Position Summary

The Reagent and Standards Administrator manages the ordering, inventory, processing, and reconciliation of laboratory reference standards and reagents. This position oversees the full chain of custody for Quality Control (QC) samples—including raw materials, finished products, in-process bulks, retain, investigation, complaint, and validation samples—from collection and logging through disposal. Additionally, the incumbent performs physical and analytical testing, maintains accurate electronic records within LIMS and database systems, and ensures strict adherence to cGMPs, Fareva specifications, and laboratory SOPs. This entry-level position operates under regular, daily supervision.

Key Responsibilities

  • Reagents & Reference Standards (70%)
    • Manage ordering, inventory levels, processing, and reconciliation of laboratory reference standards and reagents based on site usage and special requests.
    • Verify MSDS information; log, receive, label, and store materials in designated safety locations under specified storage conditions.
    • Use LIMS and physical logbooks to track, manage, and audit inventory continuous availability.
  • Sample Management & Chain of Custody (10%)
    • Oversee full sample life cycle (collection, logging, labeling, delivery, and disposal) for finished products, raw materials, bulks, retain, validation, and complaint samples.
    • Receive/collect samples from manufacturing operations and outside sources in compliance with environmental and site safety standards.
  • Assays & Analytical Testing (10%)
    • Perform physical and analytical testing on production intermediate, bulk, finished product, and process/cleaning validation samples.
    • Calculate results, interpret data, record observations, and conduct peer reviews of test data.
    • Identify basic technical issues, out-of-specification (OOS) results, and instrument malfunctions, escalating and assisting in investigations as needed.
  • Record Keeping & Documentation (5%)
    • Maintain accurate, cGMP-compliant electronic records in LIMS and database systems.
    • Perform administrative duties including shipping, receiving, and material ordering.
    • Identify atypical findings and participate in root-cause investigations under management direction.
  • SOPs & Continuous Improvement (5%)
    • Maintain up-to-date individual training records and adhere strictly to all lab SOPs.
    • Assist in writing and revising site SOPs as procedural updates occur.

Qualifications & Requirements

  • Education & Experience:
    • Bachelor’s (BS) or Master’s (MS) degree in Chemistry, Biochemistry, or a relevant science discipline.
    • 0–1 years of Quality Control/Quality Assurance experience, preferably in a bio/pharmaceutical manufacturing environment.
  • Technical & Professional Skills:
    • Basic knowledge of fundamental quality concepts, cGMP guidelines, and laboratory safety practices.
    • Working knowledge or practical application of standard analytical techniques (e.g., pH, viscosity, analytical balance, UV/Vis, FTIR).
    • Proficiency in using electronic laboratory data systems (LIMS) and database tracking tools.
    • Solid organization skills with the ability to manage daily tasks, document work accurately, and work effectively in a team environment.
  • Physical Requirements:
    • Work involves light lifting, sitting, standing, and walking across laboratory and facility environments.

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