QA Validation Engineer - Ireland, Sligo - 12 Month Contract
Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for a 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 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 and execution of the Site Validation Master Plan.
* Generation, maintenance and 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 and 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.
Seniority Level
Mid-Senior level
Employment Type
Contract
Job Function
Engineering and Information Technology
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