LIMS Developer

7 days ago

Prague, Hlavní město Praha, Czech Republic futureproof Full time 60,000 - 120,000 per year

This role is primarily technical and hands-on, focused on configuring and developing the LabWare LIMS application to meet business and regulatory requirements. The professional in this position ensures that the LIMS platform aligns with Merck's laboratory processes, integrates seamlessly with other enterprise systems (such as SAP and LabX), and delivers reliable, compliant functionality through well-structured code and configuration.

The candidate will work closely with functional analysts, business users, and QA teams to design, build, and maintain efficient laboratory information workflows. This position demands a strong understanding of both software development within LIMS and GxP-compliant systems in the pharmaceutical domain.

Key Responsibilities

  • Configure and customize LabWare LIMS based on Merck's business requirements.

  • Develop and maintain LIMS Basic code, including subroutines, automation scripts, event triggers, user programs, dialogs, and access routines.

  • Manage and modify LabWare Pharma Template configurations and static data.

  • Create, maintain, and optimize Crystal Reports for complex laboratory and compliance reporting.

  • Integrate LIMS with external systems such as SAP, LabX, and other enterprise platforms, including troubleshooting and testing of data interfaces.

  • Analyze and resolve configuration defects or performance issues.

  • Provide ongoing configuration support to site teams and assist in deployments.

  • Collaborate with QA and validation teams to ensure all system changes meet GxP and SDLC compliance standards.



Requirements
  • 5+ years of experience in LabWare LIMS configuration and development.
  • Proficiency in LIMS Basic programming, automation scripts, and event-driven architecture.
  • Hands-on experience with Crystal Reports (designing and debugging complex reports).
  • Familiarity with SAP/LIMS integration, LabX, or similar systems.
  • Strong understanding of GxP, GMP, and validation processes in pharma environments.
  • Knowledge of SDLC methodologies and change control processes.
  • Analytical problem-solving mindset with attention to data accuracy and compliance.
  • Bachelor's degree in Computer Science, Information Systems, Chemistry, or related field.


Benefits
  • Freelance contract with competitive daily rate.
  • Hybrid working regime - Prague.
  • Long-term cooperation on a global pharmaceutical project with high business visibility