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Search Results for Quality Auditor
Job Title. Location Salary Actions

Quality Manager (Healthcare)

Our client is an indigenous Pharmaceutical organisation based in Dublin who sell & distribute healthcare products across Ireland & the UK. They are currently seeking an experienced Quality Manager who will be responsible for managing the processes and systems to ensure that the company is in compliance with all applicable regulatory and business requirements. Role/Responsibilities: • Lead our clients Quality Management Systems including Documentation, Complaints Management, CAPA and Management Review. • The Quality Manager is responsible for ov...

Location: Dublin,
Quality Manager (Healthcare) 		Dublin Not Disclosed

Senior GMP Auditor

Consistently ranked as a “Top Employer” in Science Magazine’s rankings for pharmaceutical and biotechnology companies, our client offers a unique, world-class opportunity for interested candidates. An outstanding Senior GMP Auditor is required who is excited by a start-up environment and recognizes the opportunities that this offers and wants to be challenged Summary:Responsible for planning and conducting quality audits in manufacturing (GMP) within designated Quality Auditing area. Responsibilities Schedules, prepares, an...

Location: Limerick,
Senior GMP Auditor 		Limerick Not Disclosed
Other Quality Assurance Jobs
Job Title Location Salary Actions
QA Specialist Cork Not Disclosed
Quality and Customer Experience Specialist Cork Not Disclosed
Senior R&D QA Executive Galway Not Disclosed
Quality and Customer Experience Specialist Cork Not Disclosed
QA Specialist Cork Not Disclosed
QA Specialist Cork Not Disclosed
QC Lab Analyst Sligo Not Disclosed
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Quality Auditor Career Profile

Quality Auditor - Clinical Research


This is an interesting position which involves ensuring overall Quality in a Clinical Research Organisation (CRO) environment. It is a role which involves a lot of travel to various Client and supplier sites. A keen eye for detail and skill in dealing with people in required.

Main Responsibilities

  • Conducting investigator site and CRO audits
  • Carrying out the Audit of internal GCP tasks and departments
  • The maintenance of the audit log and global audit plan
  • Act as the sole Clinical QA representative on study teams that are assigned to your control
  • Performing Study document compliance audits
  • Provide GCP training to colleagues

Skills/Experience

  • A degree in health sciences, nursing, pharmacy or related field
  • Extensive experience in carrying out GCP audits in the EU inline with FDA/EMEA/global regulatory requirements and to GCP guidelines
  • A willingness to travel up to 50% of the time