LIMS Consultant

Jobtailor; Deutschland; Hybrid; EUR 60.000 - 90.000; Vollzeit

Jobbeschreibung

• Configure LIMS modules to support 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
• Travel to client sites as an integral part of the role; work from a home office when not traveling
• Deliver business solutions to clients in the life sciences, consumer products, and retail industries

Requirements

• 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
• Travel estimated at 30-50%, varying based on client and project needs

Core Competencies

Demonstrates expertise in configuring and validating LIMS modules to support laboratory workflows, with a strong focus on compliance with GxP and regulatory standards. Proficient in developing automation scripts and project documentation while collaborating effectively with cross-functional teams.

Highest-signal resume keywords

• LabWare LIMS Configuration
• LabVantage LIMS Customization
• Assay Workflow Design
• GxP Compliance Knowledge
• Regulatory Validation Experience

ATS Optimization Keywords

Hard Skills

• LIMS Configuration
• Workflow Automation Scripting
• Data Transformation
• Instrument Integration
• Project Documentation Development
• Assay Workflow Validation
• Business Rules Development
• Analytical Testing Workflows
• Sample Management
• Stability Testing

Soft Skills

• Attention to Detail
• Analytical Problem-Solving
• Effective Communication
• Collaboration Skills

Industry Keywords

• 21 CFR Part 11
• GxP
• Pharmaceuticals
• Biotechnology
• Food Safety
• Life Sciences
• Consumer Products
• Retail Industries