About Your New Company
You will be joining a global biopharmaceutical company that focus 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 own initiative.
- Strong communication skills
What is on offer as Quality Assurance Validation Engineer
- High-Rate DOE
- Experience in leading biopharmaceutical
What’s Next
Apply now by clicking the "Apply Now" button or call Elaine McCarthy at +353 21 4847135. If this job isn’t quite right but you’re looking for something similar, please get in touch. We also have multiple temporary, FTC, and contract jobs available
