LabWare LIMS Validation Specialist; Onsite

Job Title

Lab Ware LIMS Validation Specialist (Onsite role)

Please let me know if you are interested or anyone who might be interested.

Major Pharmaceutical Client

Position:
Lab Ware LIMS Validation Specialist (Onsite role)

Duration: 9+ Months (Contract)

Location:

Newbury Park (Thousand Oaks), CA 91320

Pay Rate: $90.00 – $100.00 per hour

Employment Type:

W2

• mary:
  
  Lab Ware LIMS Configuration Specialist to support a Lab Ware 8 upgrade for a 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 sys
• tems.
  
  The successful candidate will translate regulatory, quality, and operational requirements into standardized, compliant Lab Ware LIMS designs and ensure stable execution of configured Lab Ware objects following internal procedures in a regulated manufacturing environment.

• ties:
  
  Support a dedicated workstream supporting implementation of raw material and commercial product processes within Lab Ware Li
• MS 8.Define and manage Lab Ware build ac
• ross:
  
  Raw materials and commercial product master
• flows
  
  Laboratory equipment and inter

• ation
  
  Configure raw materials, commercial products including stability, and laboratory equipment in Lab Ware LIMS using standardized, compliant design patt
• erns.
  
  Ensure Lab Ware configuration aligns
• with:
  
  Approved test methodol
• ogies
  
  Product specifica
• tionsSampling
• plans
  
  Apply controlled build practices and normalized templates to ensure consistency, scalability, and compli

• support
  
  Translate regulatory, quality, and operational requirements into standardized Lab Ware LIMS des
• igns.
  
  Support validation activities by providing clear documentation and traceability for configured Lab Ware objects following internal proced

• ation
  
  Configure and support instrument interfaces between Lab Ware 8 and a variety of laboratory sys
• tems.
  
  May develop or support parsing scripts, where required and permitted by organizational standards and govern
• ance.
  
  Support connectivity and data flow between Lab Ware and other GMP systems, such as

• ution
  
  Support stable execution of raw material and equipment workflows in live operat
• ions.
  
  Troubleshoot configuration and integration issues impacting laboratory execu
• tion.
  
  Partner with site teams to ensure Lab Ware configurations are fit for intended use and operationally sustain

• Proven hands-on experience configuring Lab Ware LIMS (Lab Ware 8 strongly preferred).
• Strong experience with Lab Ware within GMP laboratory operations, particularlly:
  
  Raw materials te
• sting
  
  Commercial product te
• sting
  
  Laboratory equipment work
• flows
  
  Demonstrated ability to translate regulatory and quality requirements into compliant LIMS configurat
• ions.
  
  Experience supporting LIMS validation with full requirements traceabi

• Experience supporting Lab Ware upgrades or major LIMS implement at
• ions.
  
  Experience working in biopharmaceutical or pharmaceutical GMP environm
• ents.
  
  Experience supporting inspection readiness activities related to

• eria:
  
  Completed on-time Lab Ware LIMS configurations for raw materials, commercial products, and equipment integra
• tion.
  
  Clear requirements-to-configuration-to-validation traceabi
• lity.
  
  Stable, compliant execution of configured workflows in operat
• ions.
  
  Successful integration between Lab Ware and laboratory instrum

• notes:
  
  This role requires close collaboration with Quality, Validation, IT, and Laboratory t
• eams.
  
  Work must follow organizational change control, validation, and data integrity requirements.
• Onsite presence may be required based on project phase and site ne
• eds.
  
  This role will focus on validation document generation and liaison with onsite