QAV Engineer - Life Science - 12-Month Contract
Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for QAV Engineer to join their state of the art pharmaceutical facility.
Located in the historic province of Connacht neighbouring the pond that is the Atlantic Ocean, breeds a mix of Irish culture and modernisation in the popular seaside town rife with bars, restaurants and water sports.
Responsibilities:
1. Coordination / direction and active participation in the validation and quality assurance of site equipment, utilities, processes and software in compliance with policies, FDA, European cGMP and GAMP standards.
2. Generation/maintenance/execution of the Site Validation Master Plan.
3. Generation/maintenance/execution of Project Validation Plans and schedules.
4. Generation of validation protocols and final reports to cGMP standards.
Requirements:
5. Qualification and/or degree in engineering or scientific discipline.
6. 3 years plus validation/Quality experience in medical device plastics processing, moulding or assembly operations.
7. 3 years plus of knowledge of cGMP and regulatory requirements relating to the medical device industry.
If this role is of interest to you, please apply now
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