LabWare Specialist

About the role

The LabWare Specialist plays a crucial role in configuring, integrating, and validating LabWare LIMS within a GMP-regulated laboratory environment. This position supports end-to-end LIMS implementation activities, ensuring compliance with regulatory, quality, and operational requirements.

Responsibilities

• Configure LabWare LIMS for raw materials, commercial products, stability programs, and laboratory equipment workflows.
• Develop and maintain master data, test methods, sampling plans, and product specifications.
• Apply standardized, compliant configuration design patterns to ensure scalability, consistency, and regulatory adherence.
• Support method configuration within LabWare aligned to approved laboratory processes.
• Design, configure, and support integrations between LabWare LIMS and laboratory instrumentation (e.g., Empower, LabX).
• Enable data flow between LabWare and enterprise GMP systems.
• Support or develop parsing scripts/interfaces in alignment with system governance and standards.
• Troubleshoot integration issues and ensure reliable system connectivity and performance.
• Support Computer System Validation (CSV) activities for LabWare implementations and enhancements.
• Author and/or contribute to validation deliverables.
• Ensure full requirements-to-configuration traceability.
• Support audit readiness and ensure compliance with GxP, data integrity, and regulatory requirements.
• Gather and translate regulatory, quality, and operational requirements into standardized LabWare system designs.
• Ensure configurations align with approved test methods, specifications, and laboratory procedures.
• Partner with quality, validation, IT, and laboratory teams to ensure solutions are fit for intended use.
• Support deployment, go-live readiness, and steady-state operations of LabWare systems.
• Troubleshoot configuration and workflow issues impacting laboratory operations.
• Ensure stable execution of laboratory workflows in a GMP environment.
• Provide ongoing system support and continuous improvement recommendations.
• Collaborate with Quality, Validation, IT, and Laboratory stakeholders throughout implementation and support phases.
• Participate in requirements workshops, system design reviews, and testing activities.
• Support project timelines and deliverables as an individual contributor.

Requirements

• Bachelor’s degree in Life Sciences, Engineering, Computer Science, or related field preferred.
• 5+ years of hands-on experience with LabWare LIMS (LabWare 8 preferred) in GMP/GxP environments.
• Strong expertise in configuration of raw materials, commercial product, stability, and laboratory workflows.
• Experience integrating LabWare with laboratory systems (e.g., Empower, LabX) and supporting data interfaces.
• Proven experience supporting Computer System Validation (CSV) and authoring validation documentation (e.g., URS, IQ/OQ/PQ, traceability).
• Solid understanding of GMP, GxP, data integrity, and validation lifecycle requirements.
• Strong troubleshooting, problem-solving, and cross-functional communication skills.
• Experience with LIMS upgrades, large-scale implementations, and/or inspection readiness is preferred.

Qualifications

• Must be authorized to work in the U.S.

Skills

• Hands-on experience with LabWare LIMS
• Expertise in configuration and integration of LabWare LIMS
• Strong knowledge of Computer System Validation (CSV)
• Ability to troubleshoot and resolve integration issues
• Excellent communication and collaboration skills

Benefits

W2 Temp roles include our Medical and Sick Time benefits. The salary offered may be adjusted based on various factors such as the applicant's qualifications, skills, and professional experience.

Pay

$85,000 - $115,000 annually

Schedule

Full-time