About The Position

Seeking an experienced LabWare LIMS Configuration Specialist to support a LabWare 8 implementation in a GMP laboratory environment. The role focuses on configuring raw material, commercial product, stability, and instrument integration workflows, as well as supporting validation activities. Success is measured by timely completion of LabWare 8 configurations, successful support of validation and testing, stable execution of configured workflows in the laboratory, and successful integration of laboratory instruments and systems.

Requirements

  • Hands-on experience configuring LabWare LIMS (LabWare 7 or 8).
  • Experience in GMP-regulated laboratory environments.
  • Experience with one or more of the following: raw material testing, commercial product testing, stability programs, or 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.

Nice To Haves

  • Experience supporting LabWare 8 upgrades or LIMS implementations.
  • Pharmaceutical or biotechnology industry experience.
  • Familiarity with GMP change control and validation processes.

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.
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