Job Title
QA Validation Engineer


Location: Sligo

**Immediate Start – 4-5 month contract**

As a QA Validation Engineer you will participate in the site Validation program as well as participating in the site Quality Assurance (QA) program. You will be involved in the validation and qualification of site equipment, utilities, processes and software in line with GAMP requirements and other site specific standards.

Responsibilities

  • Generation, maintenance, and execution of the site Project Validation Plan
  • Quality Assurance of validation investigations
  • Development and execution of solutions for identified noncompliance incidents
  • The creation, review, and approval of validation documents such as FRS and DS documents
  • Management of validation and change control processes
  • Documentation in line with GMP requirements
  • Continuous improvement activities
  • Escalation of noncompliance issues and events to management

Requirements

  • Bachelor’s degree in Computer Science, Electrical Engineering, Systems Engineering, Technology or a related discipline
  • Over 3 years’ experience as a Validation / QA Engineer in the Pharmaceutical or related Healthcare industry
  • GMP environment experience and an understanding of pharma sector regulatory requirements
  • Ideally strong commissioning and qualification experience
  • Experience of GxP Computerised Systems
  • Strong prioritization and project management skills

Why Choose This Role & SL Controls

  • An excellent compensation package which rewards high performers
  • The opportunity to work clients who are global leaders in their field
  • A supportive environment committed to employee development and wellness
  • The opportunity to work with, help develop and improve upon industry leading technology solutions
  • A collaborative and open culture where you are valued and can 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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