
Lims Consultant
16 hours ago
Role & responsibilities
- Review source documentation for master data objects such as laboratory methods and analysis
- Create/ build master data objects in the LIMS, including test methods, specifications, sample plans, and instruments
- Ensure data consistency, accuracy, and compliance with internal SOPs and external regulatory requirements (e.g., FDA, ISO, GxP)
- Support LIMS validation activities, including documentation and testing.
- Troubleshoot and resolve data-related issues within the LIMS
- Collaborate with a team of master data builders working across various sites for the LIMS deployment
Preferred candidate profile
2+ years of experience working with LIMS platforms (Ideally, Caliber)
Strong understanding of laboratory operations and data management principles
Experience with master data configuration for LIMS systems
- Excellent attention to detail and problem-solving skills
- Strong communication and collaboration abilities
- Experience in a regulated industry (e.g., pharmaceuticals, biotech, food safety)
- Knowledge of GxP, 21 CFR Part 11, and other regulatory frameworks
- Bachelors degree in Life Sciences, Information Technology, or a related field
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