About Your New Company You will be joining a global biopharmaceutical company that focus on developing, and commercializing products contributing to oncology and eye 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 Abb Vie policies, FDA, EU c GMP, and GAMP standards.
Develop and manage Site Validation Master Plans and Project Validation Plans, including timelines.
Create validation protocols, reports, and investigations, ensuring c GMP 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 c GMP compliance in production areas.
What skills/experience you need as a Quality Assurance Validation Engineer Bachelors degree in engineering or scientific discipline 3 years plus of knowledge of c GMP, validation and regulatory requirements relating to the biopharmaceutical industry.
Ability to work as part of a team or on own initiative.
Strong communication skills What is on offer as Quality Assurance Validation Engineer High-Rate DOE Experience in leading biopharmaceutical Whats Next Apply now by clicking the "Apply Now" button or call Elaine Mc Carthy at.
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We also have multiple temporary, FTC, and contract jobs available Skills: GMP quality assurance validation c GMP Pharmaceutical Benefits: See Description