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Auditor, Quality Assurance

  1. Sofia, Prague, Dublin, Warsaw, Johannesburg, Barcelona, Reading
JR111211
  1. Quality Assurance
  2. ICON Full Service & Corporate Support
  3. Hybrid: Office/Remote

About the role

This vacancy has now expired. Please see similar roles below...

Locations possible : Poland, Bulgaria, South Africa, UK, Ireland, Spain and Czech Republic

This role is open to Clinical Research Associates, QA auditors and comparable roles.

GCP experience is mandatory for this role.

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.

Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Your role :

As part of the inspections team, you will be responsible for Regulatory Authority Inspection activities in the EU and APAC. This includes supporting operational teams with inspection preparation / readiness activities, managing and/or hosting Regulatory inspections of ICON or our investigator sites and supporting client inspection activities.

Additionally, you will support internal and external Clients developing Root Cause Analysis and Corrective Action and Preventive Action (CAPA) Plans to address Non-conformances identified during Regulatory Inspections.

We are looking for a new team member to join this fantastic team!

Ideally you have a good understanding of GCP and extensive clinical trial experience.

Previous experience in Regulatory inspections would be an advantage.



Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

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