About Your New Company
You will be joining a global biopharmaceutical company that focuses on developing and commercializing products contributing to oncology and eye care. This role is a 12-month contract in Sligo. As a QA Validation Engineer, you will coordinate the development and maintenance of the site validation program and ensure quality requirements are met.
About your new job as a Quality Assurance Validation Engineer
* Lead and participate in validating site equipment, utilities, processes, and software in line with AbbVie policies, FDA, EU cGMP, and GAMP standards.
* Develop and manage Site Validation Master Plans and Project Validation Plans, including timelines.
* Create validation protocols, reports, and investigations, ensuring cGMP compliance.
* Approve quality documents and manage validation, exceptions, and change control processes.
* Track validation equipment and complete required training prior to task execution.
* Update procedures and documentation to ensure best practices and provide cross-training within the team.
* Contribute to continuous improvement in manufacturing, quality, safety, and training systems.
* Communicate with management and peers to ensure cGMP compliance in production areas.
What skills/experience you need as a Quality Assurance Validation Engineer
* Bachelor’s degree in engineering or scientific discipline.
* 3 years plus of knowledge of cGMP, validation, and regulatory requirements relating to the biopharmaceutical industry.
* Ability to work as part of a team or on your own initiative.
* Strong communication skills.
What is on offer as Quality Assurance Validation Engineer
* High-Rate DOE.
* Experience in leading biopharmaceutical projects.
What’s Next
Apply now by clicking the "Apply Now" button or call Elaine McCarthy at +353 21 4847135.
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