LabWare LIMS-LES Developer

Macpower Digital Assets Edge LLC
Raleigh, NC, United States
2 days ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Compensation
$114,400.0
Working hours
Regular working hours

Tech stack

Data Integrity Relational Databases Middleware Laboratory Information Management Systems Performance Tuning Standard Sql Requirements Management System Testing Scripting Information Technology Integration Frameworks GXP

Job description

Job Summary: We are looking for a skilled LabWare LIMS-LES Developer to support and enhance our LabWare-based Laboratory Information Management System (LIMS) and Lab Execution System (LES). The ideal candidate will have hands-on experience in configuring, customizing, and maintaining LabWare LIMS/LES solutions, along with providing technical support to ensure smooth laboratory operations. We have two opening, one for each location listed below, * Design, develop, and configure LabWare LIMS and LES applications based on business requirements.

  • Customize workflows, templates, and reports using LabWare tools and scripting languages.
  • Provide ongoing support and troubleshooting for LabWare LIMS/LES-related issues.
  • Collaborate with lab users, QA, and IT teams to gather requirements and deliver effective solutions.
  • Ensure data integrity, regulatory compliance (GxP, FDA, etc.), and adherence to company SOPs.
  • Perform system testing, validation, and documentation according to defined protocols.
  • Participate in upgrades, patches, and performance optimization of the LabWare system.

Requirements

Labware, Laboratory Information Management System (LIMS), Labware, Laboratory Operations, Technical Support, Laboratory Information Management System (LIMS), Scripting (Scripting Languages), Identify Issues, Quality Assurance, Requirements Management, * Proven experience as a LabWare LIMS-LES Developer in a regulated environment.

  • Strong understanding of LIMS and LES concepts, especially in LabWare architecture.
  • Hands-on experience with LabWare scripting, visual workflows, templates, and instrument integration.
  • Familiarity with system validation (CSV), change control, and regulatory requirements (FDA 21 CFR Part 11, GxP).
  • Good analytical and troubleshooting skills.
  • Ability to communicate effectively with both technical and non-technical stakeholders.
  • Bachelor’s degree in Computer Science, Life Sciences, or a related field.

Nice to Have:

  • Experience with LabWare Pharma Template.
  • Knowledge of SQL and relational databases.
  • Familiarity with integration tools and middleware used in laboratory environments.

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