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Senior QC Specialist

Location: Dublin
Experience:See description
Job Type:Fixed Term Contract
Salary:Not Disclosed
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May be suitable for: QA Specialist

We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.


This job specification outlines the general responsibilities associated with the role of QC Investigations Specialist. The successful candidate will join the investigations team as a senior member of the team. Continuous Improvement with regard to investigations and error management will be key areas of focus for the role. 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
• Champion for Investigations in Quality Control
• Owns and Manages Investigations for QC through QMTS
• Authors and reviews investigation reports
• 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
• Seeks out opportunity to improve the process and management of Investigations
• SME for error management and error reduction in QC
• Lead improvement initiatives as required e.g. PPI
• Strong focus on RFT and Lean
• Key contact for Investigation Metrics
• Provides coaching, support and mentoring on investigations to the investigation team
• Responsible for on time co-ordination of QC Investigation Trend reports
• Builds relationships and partners with similar roles at ADL and in the network to share lessons learned and improvements
• May own Change Controls linked to investigations and CAPAs
• May provide support for Protocol generation linked to QC Investigations
• Supports Audits and Inspections with regard to preparation and participation
• Represents QC at site and network level with regard to Investigations and Error Management.
• Works with minimal supervision but knows when to escalate or look for support
• May co-ordinate the Investigation team workload such that investigations are prioritized as required and delivered within due dates. Escalates as required.:

Education & Experience

• Hold a third level qualification in Science related discipline
• Have minimum 6 years’ experience in Biotechnology/ Pharmaceutical setting
• Possess key competencies to include Planning and Organisation, Communication, Teamwork, Flexibility
• Excellent Technical Writing skills
• Proficient in Root Cause Analysis
• Detailed knowledge of the QC function and is operationally savvy
• Proven Experience of handling GMP investigations within a Quality System
• Demonstrated Leadership attributes: Delivers Results
• Knowledge of Error Management Methodologies and experience with Six Boxes Approach advantageous


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