QC Instrumentation Engineer (12-Month Contract)
We are currently seeking a QC Instrumentation Engineer to join a leading biopharmaceutical manufacturing site in Dublin 15 on a 12-month contract. This is an excellent opportunity to work within a high-performing Quality Control environment, supporting critical laboratory instrumentation and ensuring compliance with GMP standards.
Key Responsibilities
Manage the purchase, installation, qualification, and lifecycle of QC laboratory instruments
Provide calibration and maintenance services, including scheduling and tracking activities
Review and approve documentation related to instrument qualification, calibration, and repairs
Lead and manage instrument‑related investigations, including calibration deviations
Trend and monitor instrument performance and lifecycle dataSupport new instrument introduction and qualification projects
Collaborate with cross‑functional teams including QC, QA Validation, and CSV
Liaise with vendors and global stakeholders on instrumentation activities
Ensure compliance with GMP, Data Integrity (21 CFR Part 11 / EU Annex 11) and internal procedures
Contribute to the development and improvement of instrumentation procedures
Troubleshoot complex instrumentation issues within the QC laboratory
Qualifications
B.Sc in a scientific discipline (or related field)
Minimum 3 years experience in a GMP environment
At least 1 year of hands‑on instrument qualification experience
Strong understanding of laboratory instrumentation lifecycle management
Knowledge of Data Integrity requirements (21 CFR Part 11 / EU Annex 11)
Familiarity with biopharmaceutical drug substance and drug product testing
Understanding of protein biochemistry
Experience supporting technology transfers
What We’re Looking For
Strong team player with the ability to collaborate across functions
Excellent organisational and time management skills
Ability to manage multiple priorities and projects simultaneously
Clear and effective communication skills
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