LIMS Consultant

Clarkston Consulting

LIMS Consultant configuring and validating LabWare or LabVantage systems for Clarkston Consulting’s regulated life sciences clients. Supporting workflows, automation, documentation, and deployment across client sites.

Posted 8/4/2026full-timeAtlanta • Florida, Missouri, Pennsylvania, Texas • 🇺🇸 United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in configuring and customizing LabWare or LabVantage LIMS for laboratory workflows, ensuring compliance with GxP and 21 CFR Part 11 regulations. Proficient in developing automation scripts and project documentation while collaborating effectively with cross-functional teams.

Highest-signal resume keywords

LabWare LIMS ConfigurationLabVantage LIMS CustomizationAssay Workflow DesignGxP Compliance KnowledgeProject Documentation Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

LIMS ConfigurationWorkflow Automation ScriptingData TransformationAssay ValidationLaboratory Operations Understanding

Soft Skills

Attention to DetailAnalytical Problem-SolvingEffective CommunicationCollaboration Skills

Industry Keywords

Life SciencesPharmaceuticalsBiotechnologyFood Safety21 CFR Part 11

About the role

Key responsibilities & impact

Deliver creative business solutions to market-leading clients in the life sciences, consumer products, and retail industries
Configure LIMS modules supporting assay development, plate results, sample management, stability, and analytical testing workflows
Design, configure, and validate assay workflows aligned with scientific requirements and regulated GxP environments
Develop and maintain scripts for workflow automation, business rules, calculations, instrument integration, and data transformation within LIMS
Develop project documentation and conduct configuration demonstrations for clients
Collaborate with scientists, QA/CSV teams, and IT to gather requirements, design technical solutions, and support URS, FRS, DS, IQ/OQ/PQ validation activities
Ensure configurations comply with 21 CFR Part 11 and other validation procedures
Collaborate with LIMS consultants across various sites for LIMS deployment

Requirements

What you’ll need

Minimum of 2 years of hands-on experience working with LabWare or LabVantage LIMS
Experience configuring and customizing LabWare or LabVantage LIMS for laboratory workflows
Ability to design, configure, and validate assay workflows
Experience developing and maintaining scripts for workflow automation, business rules, calculations, instrument integrations, and data transformations
Solid understanding of laboratory operations and end-to-end lab processes
Proficiency in comprehensive project documentation and client configuration demonstrations
Experience in regulated environments such as pharmaceuticals, biotechnology, or food safety
Strong knowledge of GxP, 21 CFR Part 11, and other applicable regulatory requirements
4-year degree in Life Sciences, Information Technology, or a related discipline
Ability to travel an estimated 30–50%
Strong attention to detail, analytical and problem-solving skills
Effective communication and collaboration across cross-functional teams

Benefits

Comp & perks

Comprehensive Health and Wellness Benefits (Medical, Dental, Vision, and more)
401k with company contributions
Paid vacation, personal days, holidays, and sick leave
Paid Parental Leave and Family Building Benefits (Adoption, Surrogacy, and Infertility Support)
Life and Disability Insurance
Training and Professional Development investments
Tuition Assistance
Support for interview-process accommodations upon request