Job Description
This senior QC role involves overseeing laboratory operations, ensuring compliance with regulatory requirements and providing technical leadership. The successful candidate will lead a team of QC analysts, oversee complex testing methods and contribute to product quality, regulatory compliance and continuous improvement initiatives.
Key Responsibilities
* Supervise day-to-day QC laboratory operations and ensure timely and accurate testing results.
* Provide technical expertise in HPLC, GC, method validation and analytical troubleshooting.
* Lead the preparation and review of validation protocols, reports, SOPs and compliance documentation.
* Oversee instrument qualification, calibration and maintenance activities.
* Manage data integrity processes, including LIMS and CSV compliance.
* Ensure QC operations meet GMP standards and inspection readiness requirements.
Required Skills and Qualifications
* 10+ years experience in QC laboratories within the Irish pharmaceutical sector, preferably in Oral Solid Dosage.
* Strong expertise in HPLC and GC, with proven experience in method validation and protocol/report writing.
* Solid knowledge of CSV, instrument qualification and LIMS systems.
* Demonstrated leadership skills with prior experience supervising or mentoring QC teams.
* In-depth knowledge of Irish and international pharma regulations (GMP, GLP, ICH).
About the Position
This is an exciting opportunity for an experienced professional to take ownership of laboratory operations, drive compliance and provide technical leadership. If you are looking for a challenging role that aligns with your career goals, we encourage you to apply.