Responsibilities
- Assist with LabVantage system configuration under guidance from senior consultants
- Support testing activities, including writing test cases, executing scripts, and documenting results
- Help prepare user documentation, training materials, and job aids for client teams
- Provide first-line troubleshooting and issue triage for LabVantage users
- Participate in data migration activities, such as data preparation, validation, and cleanup
- Collaborate with business users to gather requirements and document workflows
- Maintain project documentation, meeting notes, and status updates
- Learn and apply relevant regulatory standards (e.g., GxP, Part 11) in daily work
Required Education
Bachelor or higher within pharma, microbiology, chemistry, or IT
Required Experience
Minimum 2 years preferable 3-5
Required Technical Skills
- Familiarity with pharmaceutical, biotech, or life sciences laboratory processes and workflows
- Prior internship, co-op, or project experience in pharmaceutical/biotech IT systems
- Basic understanding of Laboratory Information Management Systems (LIMS)
- Experience with data entry, reporting, or system-based documentation in a regulated environment
- Comfort with IT systems, troubleshooting, and user support in a lab or business setting
- Exposure to GxP, FDA 21 CFR Part 11, or other regulatory requirements in life sciences
Additional Experience And/or Skills
- French and Spanish a plus but not a requirement
- Hands-on exposure to LabVantage LIMS configuration or testing
- Experience with scripting, automation, or system integrations (e.g., Python, Java, or web services)
- Knowledge of laboratory instruments and instrument integration with LIMS
- Familiarity with SQL, relational databases, or data migration projects
- Understanding of laboratory quality systems (QA/QC) or electronic lab notebooks (ELNs)
Seniority level
Employment type
Job function
- Consulting, Information Technology, and Sales
- Industries: Pharmaceutical Manufacturing