Improve efficiency, reporting, and compliance of Laboratories by enhancing LIMS Platform stability and usability, and prepare QC labs for full digitalization through standardization and streamlining.
Requirements
- software development experience with Labware LIMS Basic.
- Labware Administration experience with expertise in Labware concepts, including subroutines, calculations, automation scripts, and message engine.
- Extensive SQL Knowledge to extract data from Labware.
- Optional experience in other code or configuration software(s).
- Experience in Pharma Industry and cGMP practices.
Responsibilities
- Customize, Configure and Maintain Labware LIMS per Business Requirements.
- Develop and Maintain Interfaces to Labware LIMS.
- Perform System Development Lifecycle (SDLC) activities including translation of requirements into Design.
- Assist with Development and User Acceptance Testing.
- Coordination of Development Resources and Activities.
Other
- minimum of 10 years making a difference in a Pharmaceutical, Scientific, Technology, Engineering, and/or Mathematics field.
- Certification in Labware Administration and/or Labware LIMS Basic preferable.
- Experience influencing, direct authority, navigating complex or matrix organizations and successfully networking and forming partnerships with cross-functional teams.
- Good Communication Skills including fluency in English
- 10% Travel Requirements
