LabWare LIMS Implementation & Validation Support Contractor (LabWare 8)
Riva Scientific · Thousand Oaks, CA · 2 mo ago
Information TechnologyContract
About the Role
Support implementation activities for a LabWare 8 upgrade in a GMP laboratory environment, with a focus on validation support, documentation coordination, requirements traceability, and deployment readiness across configuration and instrument integration workstreams. Partner cross-functionally with Quality, Validation, IT, and laboratory teams to support compliant rollout and execution.
Responsibilities
- Support implementation activities tied to LabWare LIMS configuration and instrument integration workstreams
- Coordinate documentation, testing support, and requirements traceability activities
- Assist with generation and maintenance of implementation and validation-related documentation
- Partner with Quality and Validation teams to support compliant deployment activities
- Support iterative updates, testing cycles, and issue resolution during project execution
- Help ensure configured workflows and integrations are operationally sustainable in GMP laboratory environments
- Participate in deployment readiness, defect tracking, and change management activities
- Support communication and coordination across technical and business stakeholders
Required Experience
- Experience supporting LabWare LIMS projects within regulated GMP environments
- Understanding of validation processes, traceability, and regulated documentation practices
- Experience supporting implementation, testing, or deployment activities for LIMS or laboratory systems
- Strong coordination and communication skills across Quality, IT, Validation, and laboratory teams
- Ability to work in fast-paced implementation environments with minimal onboarding
- Pharmaceutical or biopharmaceutical industry experience preferred
Preferred Experience
- Exposure to LabWare 8 upgrades or large-scale LIMS implementations
- Experience supporting both configuration and integration project teams
- Familiarity with GMP data integrity and change control processes