LabWare LIMS Configuration & Integration Specialist (LabWare 8)

Job Title: LabWare LIMS Configuration & Integration Specialist (LabWare 8)

Must be on site in california 5x a week- the onsite location is in Thousand Oaks CA

MUST HAVES:
Proven hands on experience configuring LabWare LIMS (LabWare 8 strongly preferred).
Strong experience with Labware within GMP laboratory operations, particularly:
Raw materials testing
Commercial product testing
Laboratory equipment workflows
Demonstrated ability to translate regulatory and quality requirements into compliant LIMS configurations.

Type: Contractor / Consultant

Location: (ONSITE) 100% ONSITE

Summary

Seeking an experienced LabWare LIMS Configuration Specialist to support a LabWare 8 implementation in a GMP laboratory environment. The role will focus on configuration of raw material, commercial product, stability, and instrument integration workflows, along with support for validation activities.

Responsibilities

• Configure LabWare LIMS 8 objects, workflows, master data, specifications, and test templates.
• Support implementation of raw material, commercial product, and stability workflows.
• Configure and support laboratory equipment and system interfaces.
• Translate business, laboratory, and quality requirements into compliant LabWare configurations.
• Support requirements traceability, testing, validation, and change control activities.
• Troubleshoot configuration and integration issues.
• Work with Quality, Validation, IT, and laboratory teams to support successful deployment and operation of LabWare.

Required Qualifications

• Hands-on experience configuring LabWare LIMS (LabWare 8 preferred).
• Experience in GMP-regulated laboratory environments.
• Experience with one or more of the following:
  • Raw material testing
  • Commercial product testing
  • Stability programs
  • Laboratory equipment integration
• Experience supporting LIMS validation and testing activities.
• Experience with laboratory systems such as LabX, Empower, or similar platforms.
• Strong documentation and communication skills.

Preferred Qualifications

• Experience supporting LabWare8 upgrades or LIMS implementations..
• Pharmaceutical or biotechnology industry experience.
• Familiarity with GMP change control and validation processes.

Success Measures

• Timely completion of LabWare 8 configurations.
• Successful support of validation and testing activities.
• Stable execution of configured workflows in the laboratory environment.
• Successful integration of laboratory instruments and systems.