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LIMS Consultant
Clarkston Consulting. Configure LIMS modules to support workflows, including assay development, plate results, sample management, stability, and analytical testing processes .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in configuring and validating LIMS modules to support laboratory workflows, with a strong focus on compliance with GxP regulations and 21 CFR Part 11. 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 Design and ValidationGxP Compliance KnowledgeRegulatory Requirements Expertise
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
LIMS ConfigurationWorkflow Automation ScriptingData TransformationAssay DevelopmentInstrument IntegrationProject Documentation DevelopmentValidation ProceduresLaboratory Operations UnderstandingBusiness Rules DevelopmentAnalytical Testing Processes
Soft Skills
Attention to DetailAnalytical Problem-SolvingEffective CommunicationCollaboration Skills
Industry Keywords
GxP21 CFR Part 11PharmaceuticalsBiotechnologyFood Safety
About the role
Key responsibilities & impact- Configure LIMS modules to support workflows, including assay development, plate results, sample management, stability, and analytical testing processes
- 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 system validation activities (URS, FRS, DS, IQ/OQ/PQ)
- 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 to support laboratory workflows
- Proven 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
- Proficient in developing comprehensive project documentation and delivering configuration demonstrations to clients
- Excellent attention to detail with strong analytical and problem-solving skills
- Effective communication and collaboration skills, with the ability to work across cross-functional teams
- Experience working 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
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, and more
- Home office work when not traveling or at a client site
- Relocation is not required