QAV Engineer

QAV Engineer - Ireland, Sligo - 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. 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.

Essential duties and responsibilities for this role include, but are not limited to, the following:

• 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/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.

Desirable Experience:

• Qualification and/or degree in engineering or scientific discipline.
• Requires extensive validation/Quality experience in medical device plastics processing, moulding or assembly operations.
• 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!
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