LabWare LIMS Integration Specialist

Katalyst CRO; Thousand Oaks (CA); On-site; USD 90,000 - 135,000; Full time

Job summary

Katalyst CRO in Thousand Oaks, CA seeks an experienced LabWare LIMS Configuration Specialist to support a LabWare 8 implementation in a GMP laboratory. The role focuses on configuring raw material, commercial product, stability workflows, and integrating instruments.

Responsibilities include translating requirements into compliant LabWare configurations, supporting validation activities, testing, and change control, and collaborating with Quality, Validation, IT, and lab teams to ensure a

Qualifications

• Hands-on LabWare LIMS configuration experience.
• Experience in GMP-regulated laboratory environments.
• Experience with LabWare8 upgrades or implementations.
• Familiarity with LabX or Empower laboratory systems.

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.

Skills

LabWare LIMS configuration

GMP experience

LabWare8 familiarity

Documentation & communication

Tools

LabX

Empower

Job description

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.

Must Have's

• Configuration experience in Configuring LABWARE 8.


• Support implementation of raw material, commercial product, and stability workflows.


• Configure and support laboratory equipment and system interfaces.