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LabWare 8 LIMS Configuration & Integration Specialist


Job Location:

California, CA - USA

Monthly Salary: Not provided by the employer
Posted: 5 June 2026 (30+ days ago)
Application Deadline: 2 September 2026
Vacancies: 1 Vacancy
The job posting is outdated and position may be filled

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.