LIMS Business Analyst
About The Position
We are seeking a detail-oriented and collaborative LIMS Business Analyst to support the deployment of a new laboratory information management system within an Analytical Sciences environment. The ideal candidate will have experience working closely with scientific teams to translate complex laboratory processes into structured system solutions. This individual will act as a bridge between laboratory operations and digital platforms, ensuring workflows are accurately configured, validated, and aligned with regulatory standards. A strong understanding of GMP environments, data integrity, and system configuration is essential.
Requirements
- Experience as a Business Analyst, preferably within LIMS, laboratory systems, or scientific environments
- Strong understanding of laboratory workflows, analytical methods, and data processes
- Experience working in GMP-regulated environments with knowledge of FDA cGMP and 21 CFR Part 11 requirements
- Hands-on experience with system configuration, UAT, and requirements gathering
- Ability to translate complex scientific processes into structured digital solutions
- Familiarity with LIMS platforms or similar laboratory software (low-code environments preferred)
- Experience supporting system implementation, upgrades, or migrations
- Strong communication skills with the ability to work closely with scientists, technical teams, and stakeholders
- Detail-oriented with strong problem-solving and analytical thinking skills
- Ability to manage multiple priorities and work effectively in a fast-paced, collaborative environment
Responsibilities
- Partner with analytical scientists and subject matter experts to understand and document laboratory methods and workflows
- Translate scientific processes into structured method templates using a low-code platform
- Configure workflows, methods, and system logic within the LIMS environment (no coding required)
- Develop, execute, and document user acceptance testing (UAT) to ensure system functionality meets requirements
- Identify and support resolution of system gaps between current processes and the new platform
- Assist with configuring instrument connectivity and data capture across laboratory systems
- Ensure all system configurations and processes comply with FDA cGMP and data integrity standards (including 21 CFR Part 11)
- Collaborate with cross-functional teams to align system standards, documentation, and best practices
- Contribute to knowledge transfer efforts and support documentation for system readiness and ongoing use
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
