Quality Assurance Validation Engineer
We are seeking a skilled professional to join our team at a state-of-the-art pharmaceutical facility in Sligo, Ireland. As a QAV Engineer, you will be responsible for ensuring the quality and compliance of site equipment, utilities, processes, and software with industry standards.
Responsibilities:
* Coordinate and participate in the validation and quality assurance of site equipment, utilities, processes, and software.
* Develop and maintain Site Validation Master Plans, Project Validation Plans, and schedules.
* Generate validation protocols and final reports to cGMP standards.
Requirements:
* A degree in engineering or scientific discipline is required.
* At least 3 years of experience in validation/quality assurance in medical device plastics processing, moulding, or assembly operations.
* Extensive knowledge of cGMP and regulatory requirements relating to the medical device industry.
About the Role
This is an exciting opportunity to work with innovative solutions in the life science industry.