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QA Validation Engineer

  1. Ireland, West
Sligo
  1. Contract
Competitive
  1. Life Sciences
38555
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QA Validation Engineer - Ireland, Sligo - 12 Month Contract

Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for an QA Validation Engineer to join their state-of-the-art pharmaceutical facility. They have invested $55 billion in research to discover and develop new medicines in the pursuit of scientific breakthroughs and changing people’s lives. They have 50,000 employees around the world and are continuing to grow.

What you'll do:
  • Coordination / direction and active participation in the validation and quality assurance of site equipment, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
  • Generation/maintenance/execution of the Site Validation Master Plan.
  • Generation/maintenance/execution of Project Validation Plans and schedules.
  • Generation of validation protocols and final reports to cGMP standards.
  • Generation of validation investigations and implementation of corrective actions.
  • Creation/Review/Approval of various quality documents and test data.
What you'll need:
  • Qualification and/or degree in engineering or scientific discipline.
  • Extensive validation/Quality experience in medical device plastics processing, moulding or assembly operations.
  • Strong knowledge of cGMP and regulatory requirements relating to the medical device industry.
  • Strong communication (written and oral), presentation and troubleshooting skills required
  • Effective interpersonal and organisational skills.
  • Ability to work well both independently and in a team environment.
  • Capable of prioritising work and multitasking
If this role is of interest, please apply now!
#LI-CB1
 


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