Sr. Associate QC Systems
Amgen · Dublin, Ireland
QualityFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Associate role supporting quality control investigations at Amgen's Dublin facility. The position involves managing the complete lifecycle of quality records, including deviation investigations, corrective actions, and change controls, with emphasis on technical documentation and root cause analysis.
What they're looking for
- Third-level qualification in science-related discipline
- Minimum 4 years biotechnology or pharmaceutical industry experience
- GMP investigation experience within quality systems preferred
- Detailed knowledge of QC function and operational processes
- Strong written and verbal communication with technical writing capability
What you'll be doing
- Own and manage end-to-end investigation lifecycle through DQMS system
- Author and review investigation documents with focus on robust CAPA development
- Participate in investigation triage and ensure compliance with procedures
- Support audits and inspections; represent QC at site and network level
- May manage change controls linked to investigations and identify process improvements
Compensation€52,756.95–€71,377.05 annual
Privacy & handoff
This role links to Amgen's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.