QAV Specialist - (Hybrid) 2/3 days per week - Carlow - 11-Months
With worldwide demand for their life-changing oncology treatment increasing; one of our global pharmaceutical clients is looking for a QAV Specialist to join their team to support multiple capital projects taking place onsite in Carlow.
This is a fantastic opportunity to work on a state-of-the art fill-finish facility and the company’s first stand-alone vaccine and biologics plant outside the US.
Role summary:
- Provide quality oversight and direction for the introduction of new products.
- Conduct quality reviews and approvals of engineering/validation/automation/utilities commissioning and qualification activities.
- Author, review, and approve protocols and reports for technology transfer, method qualification, and method validation.
Requirements:
- A minimum of 3-5 years of experience in a quality role, ideally in a pharmaceutical manufacturing environment
- Quality oversite experience in reviewing and approving documents associated with Equipment Validation, Cleaning validation, Sterilization such as Autoclaves and other equipment like CTU's, Isolators etc.
- Also looking for Quality oversite of equipment Qualification and knowing how to review and approve the following documents IQ, OQ, PQ, IOC, IOQ's etc.
- If they have used these systems also would be great KNEAT, IPI, Veeva Vault.
If you are interested, please apply now for immediate consideration and further information.
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