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Sr. Associate QC Systems

Amgen

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  1. Why do you want to join Amgen?
  2. Tell me about a problem you solved at work that you are proud of.
  3. Tell me about a time you disagreed with your manager. What happened?
  4. Where do you want to be in three years?
  5. What is a weakness you are working on, and how?

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Career Category Quality Job Description Overview: This job specification outlines the general responsibilities associated with the role of Senior Associate, Quality Control, Investigations at Amgen Dun Laoghaire. The QC Systems team provide support to the QC function for all activities within Amgen’s Quality System associated with QC Deviation Investigations, CAPA records, Testing Results Assessments (TRA) and Change Controls. The successful candidate will own and manage the end-to-end life cycle of Quality records on behalf of Quality Control. The role has a strong focus on technical writing and problem-solving including Root Cause Analysis and 5 Why methodologies. Additionally, the role may involve carrying out additional work functions that are not described in this specification but are associated with the QC support function. Key Responsibilities: Owns and Manages Investigations for QC through DQMS. Author and review investigation documents. Participates routinely in the investigation triage process. Ensures investigations are kept up to date and compliant with procedures. Ensure investigations result in robust CAPA to prevent recurrence. Seeking out opportunity to improve the process and management of Investigations. Strong focus on RFT and Lean. Build relationships and partners at ADL and in the network. May own Change Controls linked to investigations and CAPAs. Supports Audits and Inspections regarding preparation and participation Represents QC at site and network level regarding Investigations. Works with minimal supervision but knows when to escalate or look for support Knowledge and Experience Hold a third level qualification in a science related discipline Have a minimum of 4 years’ experience in Biotechnology/ Pharmaceutical setting. Proven Experience of handling GMP investigations within a Quality System an advantage. Detailed knowledge of the QC function and is operationally savvy. Excellent verbal and written communication skills including technical writing, presentation and facilitation skills. . Salary Range 52,756.95 EUR - 71,377.05 EUR

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Listed on workday · posted 2026-09-24. ApplySarthi collects openings and links to application pages; the role is advertised by Amgen, not by us.