LabWare 8 LIMS Configuration & Integration Specialist
California, CA - USA
Job Summary
Job Title: LabWare 8 LIMS Configuration & Integration Specialist
Location: Thousand Oaks CA (Hybrid Preferred) Remote Possible for Highly Qualified Candidates- Need local
Position Overview
We are seeking an experienced LabWare 8 LIMS Configuration & Integration Specialist to support a major LabWare 8 upgrade initiative for a GMP-regulated laboratory environment. The consultant will lead a dedicated workstream responsible for configuring laboratory workflows managing master data supporting system validation and integrating LabWare with laboratory instruments and enterprise GMP systems.
This is a high-impact role supporting raw material and commercial product testing operations within a regulated pharmaceutical/biopharmaceutical environment.
Key Responsibilities
- Configure and implement LabWare 8 LIMS solutions for GMP laboratory operations.
- Design and deploy workflows supporting:
- Raw Material Testing
- Commercial Product Testing
- Laboratory Equipment Management
- Configure and maintain LIMS master data specifications test methods and workflows.
- Integrate LabWare with laboratory instruments and external enterprise systems.
- Collaborate with Quality Laboratory Operations Validation and IT teams to ensure compliant system implementation.
- Translate regulatory quality and business requirements into effective and compliant LIMS configurations.
- Support system validation activities ensuring full traceability from requirements through configuration and testing.
- Assist with inspection readiness and audit support activities related to LIMS.
- Troubleshoot and resolve configuration workflow and integration issues.
- Ensure stable compliant and efficient laboratory workflows following deployment.
Required Qualifications
Must-Have Skills
- Hands-on experience configuring LabWare 8 LIMS.
- Proven track record delivering LabWare LIMS implementations and configurations on schedule.
- Strong experience supporting:
- Raw Materials Testing
- Commercial Product Testing
- GMP Laboratory Operations
- Experience configuring and managing laboratory workflows within regulated environments.
- Knowledge of GMP GxP and laboratory compliance requirements.
- Experience supporting LIMS validation activities and documentation.
- Strong understanding of requirements-to-configuration-to-validation traceability.
- Experience integrating LabWare with laboratory instrument systems such as:
- Empower
- LabX
- Similar laboratory platforms
- Excellent communication and stakeholder management skills.
- Ability to work effectively with cross-functional teams in regulated environments.
Preferred Qualifications
- Experience within pharmaceutical biotechnology or biopharmaceutical organizations.
- Experience supporting regulatory inspections and audit readiness activities.
- Prior experience leading LabWare upgrade or migration projects.
Submission Requirements
- Two recent professional references are required at the time of submission.
- Resumes will be reviewed through an AI screening process; candidates should provide accurate and authentic project experience.
- Client information will be shared after a qualified candidate has been identified and submitted.
Ideal Candidate
The ideal candidate will be a senior LabWare specialist with deep expertise in GMP laboratory operations hands-on LabWare 8 configuration experience strong integration capabilities and a proven history of delivering compliant LIMS solutions within pharmaceutical or biopharmaceutical environments.