LabWare 8 LIMS Configuration & Integration Specialist

Hi,My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.Role: LabWare 8 LIMS Configuration & Integration SpecialistLocation: Remote (California-Based Project)Duration: Through March 2027 (Potential Extension)Position OverviewWe are seeking an experienced LabWare 8 LIMS Configuration & Integration Specialist to support a large-scale LabWare 8 upgrade initiative within a GMP-regulated pharmaceutical laboratory environment. This role will lead critical workstreams focused on configuring raw material and commercial product testing workflows, master data management, equipment integration, and validation support.The ideal candidate will have extensive hands-on experience with LabWare 8 configuration, laboratory system integrations, and GMP laboratory operations, with the ability to deliver compliant and scalable LIMS solutions.Key ResponsibilitiesConfigure and implement LabWare 8 LIMS workflows supporting raw material and commercial product testing processes.Lead master data configuration and management activities to support laboratory operations.Design, configure, and optimize laboratory workflows while ensuring compliance with GMP and regulatory requirements.Support integration of LabWare 8 with laboratory instrumentation and enterprise systems.Collaborate with Quality, Validation, Laboratory Operations, and IT teams to ensure successful project execution.Translate business, quality, and regulatory requirements into compliant LIMS configurations.Support system validation activities, ensuring complete requirements-to-configuration-to-validation traceability.Troubleshoot configuration, workflow, and integration issues while driving timely resolution.Assist with user acceptance testing (UAT), system testing, and deployment activities.Support inspection readiness efforts and ensure compliance with regulatory expectations for computerized systems.Provide technical guidance and documentation throughout the project lifecycle.Required Qualifications8+ years of experience working with Laboratory Information Management Systems (LIMS).Strong hands-on experience configuring and implementing LabWare 8 LIMS.Proven experience supporting LabWare upgrades, implementations, or enhancement projects.Experience Configuring Workflows ForRaw Material TestingCommercial Product TestingLaboratory Equipment and Instrument WorkflowsDemonstrated experience supporting GMP-regulated laboratory environments.Experience integrating LabWare with laboratory instruments and enterprise systems.Strong understanding of computerized system validation (CSV) principles and documentation requirements.Experience supporting validation deliverables with end-to-end traceability.Excellent communication and stakeholder management skills within regulated environments.