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LabWare LIMS Configuration Specialist

Alpha Business Solutions

Newbury Park (Thousand Oaks), CA(remote)

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JOB DETAILS
SALARY
$70–$80 Per Hour
SKILLS
Biotech and Pharmaceutical, Change Control, Communication Skills, Cross-Functional, Data Quality, Dental Insurance, Design Patterns Programming Methodologies, Documentation, Environmental Communications, GMP (Good Manufacturing Practices), Laboratory Equipment, Laboratory Information Management System (LIMS), Laboratory Operations, Laboratory Systems, Labware, Leadership, Manufacturing, Materials Testing, Product Testing, Quality Assurance Methodology, Regulations, Requirements Validation/Verification, Scripting (Scripting Languages), Testing, Time Management, Traceability, Vision Plan
LOCATION
Newbury Park (Thousand Oaks), CA
POSTED
5 days ago
Job Title: LabWare LIMS Configuration & Integration Specialist (LabWare 8)
Location: Greater Los Angeles Area | Open to 100% Remote for non-local candidates
Duration: 9 months plus | Hybrid (2-3 days /week onsite with flexibility) | Open to 100% Remote for non-local candidates
Pay rate: $70/HR - $80/HR W2 
 
Job Summary
LabWare LIMS Configuration Specialist to support the LabWare 8 upgrade for a US based GMP laboratory site. This role will lead a dedicated workstream focused on implementing raw material and commercial product workflows, completing master data configuration, and finalizing integration with laboratory equipment and enterprise GMP systems.
The successful candidate will translate regulatory, quality, and operational requirements into standardized, compliant LabWare LIMS designs and ensure stable 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 commercial product processes within LabWare LIMS 8.
  • Define and manage LabWare build across:
  • Raw materials and commercial product master data
  • Test workflows
  • Laboratory equipment and interfaces
LabWare LIMS Configuration
Configure raw materials, commercial 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 Takeda internal procedures.
Instrument & System Integration
Configure and support instrument interfaces between LabWare 8 and a variety of laboratory systems.
May develop or support parsing scripts, where required and permitted by Takeda standards and governance.
Support connectivity and data flow between LabWare and other GMP systems, such as LabX
Operational Readiness & Execution
Support stable 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 within GMP laboratory operations, particularly:
  • Raw materials testing
  • Commercial 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:
  • Instrument systems (e.g., Empower, 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 related to LIMS.
 
Deliverables & Success Criteria
  • Completed on time LabWare LIMS configurations for raw materials, commercial products, and equipment integration.
  • Clear requirements to configuration to validation traceability.
  • Stable, compliant execution of configured workflows in operations.
  • Successful integration between LabWare and laboratory instruments
 
Additional Notes
  • This role requires close collaboration with Quality, Validation, IT, and Laboratory teams.
  • Work must follow Takeda change control, validation, and data integrity requirements.
  • Onsite presence may be required based on project phase and site needs.

 Please apply with your interest. You may also reach out to me at

abaranwal@alphambe.com


 
Thank you,
Ashu
 
We provide a comprehensive package which includes.
Benefits
  • Medical for full time employees
  • Dental, and Vision Insurance
  • Life Insurance, Short-Term Disability, Long-Term Disability, etc.
 
 

About the Company

A

Alpha Business Solutions