Digital Transformation Engineer – Quality Control Laboratory

3 days ago


Limerick, Limerick, Ireland Westbourne IT Global Services Full time

Westbourne IT Global Services is seeking a Digital Initiatives Specialist to support key digital transformation initiatives within the Quality Control Laboratory (QCL) in Limerick. This role will play a vital part in advancing the Digital Roadmap by leading efforts in data management, standardization, and system integration, collaborating with both local and global teams.

The ideal candidate will have expertise in data mapping, digital solutions deployment, and QC business processes, along with strong project management skills and the ability to coordinate between business and technical teams.

Key Responsibilities
  • Support the data mapping process within QCL and coordinate across teams to ensure accurate and consistent data structures.

  • Drive data integrity, governance, and standardization to align with business and regulatory requirements.

  • Collaborate with global teams to implement and support digital solutions, including Nymiband integration.

  • Support the local deployment, validation, and maintenance of digital tools in QCL.

  • Lead digital transformation projects, ensuring timely execution and adherence to QCL's Digital Roadmap.

  • Act as a liaison between QC teams, IT, and global stakeholders, facilitating smooth communication and adoption of new technologies.

Preferred Skills
  • QC application knowledge – Familiarity with quality control systems, workflows, and data structures.

  • QC business process knowledge – Strong understanding of QC operations, compliance, and digital initiatives in a GxP environment.

  • Business analysis – Ability to interpret outputs from diverse data systems, analyze, and present findings to business stakeholders.

  • Experience with Nymiband software and hardware or similar systems.

  • Certification in CAPM or PMP is preferred.

Required Experience & Qualifications
  • Bachelor's degree in chemistry or computer science.

  • 3-5 years of experience in a pharmaceutical manufacturing environment.

  • 2-3 years of experience in a quality control environment.

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