Quality Audit Specialist

1 week ago


Dublin, Ireland Astrazeneca Gmbh Full time

ROLE CAN BE BASED FROM ATHLONE, CORK OR DUBLIN OFFICES
Overview
Introduction to role
Are you ready to make a difference in the world of rare diseases?
As a Quality Audit Specialist, you'll be at the forefront of ensuring excellence within AstraZeneca's Alexion Rare Disease Unit.
Your role will involve managing the entire audit and inspection process, from preparation to closure, while implementing best practices and educating employees on audit management systems.
Join us in our mission to deliver quality assurance activities that support audits and health authority inspections.
Responsibilities
Deliver quality assurance activities at Alexion's GQA hub to support audits and inspections.
Support key stakeholders during audit/inspection preparation and management.
Develop and communicate audit schedules/plans.
Create audit agendas by identifying risks/issues and engaging stakeholders.
Review and issue audit reports.
Enter report/responses into the Quality Management system.
Review audit actions from receipt to closure.
Oversee outsourced activities from assignment to delivery.
Lead audit consultancy communications for audit program management.
Work independently and as part of a team.
Partner with Alexion stakeholders to collect feedback for effective audit function operation.
Act as a quality point of contact for audit/inspection queries.
Participate in continuous compliance improvement projects.
Review and approve SOPs and procedural documentation.
Act as SME/Quality contact on key Quality system records.
Support/lead audits when required.
Essential Skills/Experience
Bachelor's Degree in physical/life science or pharmacy; Advanced degree preferable
Minimum of 3 years' experience in a GxP Quality Assurance or Compliance Management related role, with Quality Management Systems knowledge
Demonstrable communication and project management skills; experience working in cross-functional teams
Strong Business Partner with a focus on collaboration and delivering results
Knowledge of applicable international GXP regulations and standards (e.g., GMP, GDP etc.)
Excellent interpersonal skills are required, as is the ability to communicate well, both verbally and written
Experience with Quality Systems/tools (e.g. Microsoft office, ECMS, EQV, SmartSheet) an advantage
Desirable Qualifications
Exposure to audits (internal, supplier or corporate) or inspectorates (e.g. HPRA, FDA, NSAI) is an advantage
Exposure to supplier quality management
Why AstraZeneca?
At AstraZeneca's Alexion Rare Disease Unit, we are driven by our passion to innovate and create meaningful value.
Our unique culture combines the entrepreneurial spirit of a leading biotech with the resources of a global biopharma.
We are committed to making a difference for patients living with rare diseases by fostering a diverse and inclusive environment where ideas flourish.
Join us in our mission to change lives for the better, every day.
Ready to embark on this exciting journey?
Apply now and be part of a team that truly makes an impact
Date Posted
25-Sep-2025
Closing Date
08-Oct-2025
Our mission is to build an inclusive and equitable environment.
We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process.
We welcome and consider applications from all qualified candidates, regardless of characteristics.
We offer reasonable adjustments/accommodations to help all candidates to perform at their best.
If you have a need for any adjustments/accommodations, please complete the section in the application form.
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