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QAV Engineer - Life Science - 12-Month Contract
Located on the picturesque west coast of Ireland, our global pharmaceutical client is looking for a QAV Engineer to join their state-of-the-art pharmaceutical facility.
Located in the historic province of Connacht, neighboring the pond that is the Atlantic Ocean, this area blends Irish culture with modernisation in a popular seaside town rife with bars, restaurants, and water sports.
Responsibilities:
* 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.
* 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.
Requirements:
* Qualification and/or degree in engineering or scientific discipline.
* 3+ years validation/quality experience in medical device plastics processing, moulding, or assembly operations.
* 3+ years 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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