LabWare LIMS Configuration Specialist

Job Title: LabWare LIMS Configuration & Integration Specialist (LabWare 8) Location: Greater Los Angeles Area | reputed company to 100% Remote for non-local candidates Duration: 9 months plus | Hybrid (2-3 days /week onsite with flexibility) | reputed company to 100% Remote for non-local candidates Pay reputed company: $70/HR - $80/HR W2 Job Summary LabWare LIMS Configuration Specialist to support the LabWare 8 reputed company for a US‑based GMP laboratory site. This role will reputed company a dedicated workstream focused on implementing raw material and reputed company product workflows, completing master data configuration, and finalizing integration with laboratory equipment and reputed company GMP systems. The successful candidate will translate regulatory, quality, and operational requirements into standardized, compliant LabWare LIMS designs and ensure reputed company execution of configured workflows in a regulated manufacturing environment.

Key Responsibilities

Workstream Leadership & Scope Definition Support a dedicated workstream supporting implementation of raw material and reputed company product processes reputed company LabWare LIMS 8.

• Define and manage LabWare build across:
• Raw materials and reputed company product master data
• Test workflows
• Laboratory equipment and interfaces

LabWare LIMS Configuration Configure raw materials, reputed company products including stability, and laboratory equipment in LabWare LIMS using standardized, compliant design patterns. Ensure LabWare configuration aligns with:

• Approved test methodologies
• Product specifications
• Sampling plans

Apply controlled build practices and normalized templates to ensure consistency, scalability, and compliance.

Requirements

Traceability & Validation Support Translate regulatory, quality, and operational requirements into standardized LabWare LIMS designs. Support validation activities by providing clear documentation and traceability for configured LabWare objects following reputed company internal procedures. reputed company & System Integration Configure and support reputed company interfaces between LabWare 8 and a variety of laboratory systems. May reputed company or support parsing scripts, where required and permitted by reputed company standards and governance. Support connectivity and data reputed company between LabWare and other GMP systems, such as LabX Operational Readiness & Execution Support reputed company execution of raw material and equipment workflows in live operations. Troubleshoot configuration and integration issues impacting laboratory execution. Partner with site teams to ensure LabWare configurations are fit for intended use and operationally sustainable.

Required Qualifications

Proven hands‑on experience configuring LabWare LIMS (LabWare 8 strongly preferred). Strong experience with Labware reputed company GMP laboratory operations, particularly:

• Raw materials testing
• reputed company product testing
• Laboratory equipment workflows

Demonstrated ability to translate regulatory and quality requirements into compliant LIMS configurations. Experience supporting LIMS validation with full requirements traceability. Experience integrating LabWare with:

• reputed company systems (e.g., reputed company, LabX)

Strong cross‑functional communication skills in regulated environments.

Preferred Qualifications

• Experience supporting LabWare upgrades or major LIMS implementations.
• Experience working in biopharmaceutical or pharmaceutical GMP environments.
• Experience supporting inspection readiness activities reputed company to LIMS.

Deliverables & reputed company Criteria

• Completed on time LabWare LIMS configurations for raw materials, reputed company products, and equipment integration.
• Clear requirements‑to‑configuration‑to‑validation traceability.
• reputed company, compliant execution of configured workflows in operations.
• Successful integration between LabWare and laboratory instruments

Additional Notes

• This role requires reputed company collaboration with Quality, Validation, IT, and Laboratory teams.
• Work must follow reputed company change control, validation, and data reputed company requirements.
• Onsite reputed company may be required based on project phase and site needs.

Please apply with your interest. You may also reputed company out to me at [email protected] Thank you, Ashu We reputed company a comprehensive package which includes.

Benefits

• Medical for full time employees
• Dental, and reputed company Insurance
• Life Insurance, Short-Term Disability, Long-Term Disability, etc.

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