LabWare LIMS Configuration & Integration Specialist

Hybrid in Thousand Oaks, CA, US • Posted 1 day ago • Updated 1 day ago
Contract Corp To Corp
Contract W2
Contract Independent
12 Months
No Travel Required
Able to Sponsor
Hybrid
Depends on Experience
Company Branding Image
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Biotechnology
  • LIMS
  • Laboratory Equipment
  • GMP
  • Pharmaceutics
  • Workflow

Summary

LabWare LIMS Configuration & Integration Specialist

Location: Newbury Park, CA (3 days/week onsite or 2 weeks/month onsite)

3 open positions

 

Must have: LABWARE 7

Highly prefer LABWARE 8

 



Seeking an experienced LabWare LIMS Configuration Specialist to support a LabWare 8 implementation in a GMP laboratory environment. The role will focus on configuration of raw material, commercial product, stability, and instrument integration workflows, along with support for validation activities.


Responsibilities

  • Configure LabWare LIMS 8 objects, workflows, master data, specifications, and test templates.
  • Support implementation of raw material, commercial product, and stability workflows.
  • Configure and support laboratory equipment and system interfaces.
  • Translate business, laboratory, and quality requirements into compliant LabWare configurations.
  • Support requirements traceability, testing, validation, and change control activities.
  • Troubleshoot configuration and integration issues.
  • Work with Quality, Validation, IT, and laboratory teams to support successful deployment and operation of LabWare.

Required Qualifications

  • Hands-on experience configuring LabWare LIMS (LabWare 8 preferred). LabWare 7 acceptable with proven experience.
  • Experience in GMP-regulated laboratory environments.
  • Experience with one or more of the following:
    • Raw material testing
    • Commercial product testing
    • Stability programs
    • Laboratory equipment integration
  • Experience supporting LIMS validation and testing activities.
  • Experience with laboratory systems such as LabX, Empower, or similar platforms.
  • Strong documentation and communication skills.

Preferred Qualifications

  • Experience supporting LabWare8 upgrades or LIMS implementations..
  • Pharmaceutical or biotechnology industry experience.
  • Familiarity with GMP change control and validation processes.

Success Measures

  • Timely completion of LabWare 8 configurations.
  • Successful support of validation and testing activities.
  • Stable execution of configured workflows in the laboratory environment.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91098630
  • Position Id: 9125718
  • Posted 1 day ago

Company Info

About Lorvenk Technologies LLC

Lorvenk Technologies , founded in Virginia-USA, is a leading provider of Custom Application Development and end-to-end IT Services to clients globally. We use a client-centric engagement model that combines local on-site and off-site resources with the cost, global expertise and quality advantages of off-shore operations. We deliver Custom Application Development, Application Modernization, Business Process Outsourcing and Professional IT Services from office locations in USA and India.

Contact the job poster
MK

Mohan Krishna

Recruiter @ Lorvenk Technologies LLC

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