Job Title
CSV Lab Engineer


Location: Dublin

In this role you will manage the execution of the lab equipment validation as per the project plans and develop and review validation plans, test protocols, test data and test reports for embedded medical devices.

Responsibilities

  • Generating validation protocols and reports in accordance with cGMP and customer requirements.
  • Execution of protocols for equipment, process, utilities, methods and computerised systems.
  • Managing the execution of the lab equipment validation as per the MVP and project plan.
  • Provide guidance to Junior validation engineers.
  • Managing the preparation, review and issuing of validation protocols and reports in accordance with cGMP and customer requirements.
  • Generating validation documentation including risk assessments, traceability matrices, and validation reports.
  • Reviewing and approving specifications associated with Equipment, Processes, Products and Computerised Systems.
  • Working directly with a cross functional team to define inputs and requirements to the MVP.
  • Reviewing and managing change control forms for Validation/Compliance implications.
  • Conducting Risk Assessments.
  • Developing and reviewing validation plans, test protocols, test data and test reports for embedded medical devices.
  • Execute test cases per protocol and document the results.
  • Provide technical direction and hands-on assistance for testing projects.
  • Reviewing vendor validation documentation.
  • Liaising with customer departments.

Requirements

  • Bachelor’s degree in Computer Science, Electrical Engineering, Systems Engineering, Technology or a related discipline.
  • Over 3-5 years’ experience as a Validation Engineer (mainly computer validation) in the Pharmaceutical or related Healthcare industry.
  • Validation experience in a lab operations environment.
  • Experience in the validation of equipment and utilities.
  • Experience of GxP Computerised Systems.
  • Industry knowledge of EU GMP (IMB/FDA), Annex 11 Computerised System Validation, ISO quality requirements.
  • Familiar with the GAMP5 guidelines.
  • Excellent communication skills, including ability to advise and influence.
  • Excellent attention to detail.
  • Excellent understanding of validation concepts and documentation.
  • Excellent communication skills, including ability to advise and influence.
  • Should be based within a commutable range or else willing to re-locate for 1 year period.

Why Choose This Role & SL Controls

  • An excellent salary and benefits package including pension and health cover and other benefits such as:
    • Educational assistance
    • Income protection scheme
    • Wellness and health initiatives
  • The opportunity to work with clients who are global leaders in their field
  • A supportive environment committed to employee development and wellness
  • The opportunity to work with and help develop and improve upon industry leading technology solutions
  • A collaborative and open culture where you are valued and have the opportunity to contribute to company initiatives and growth

About SL Controls

SL Controls are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets. Over the past 16 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Dublin and Florida. We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM’s and Technology providers.

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