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Search Results for Quality Auditor
Job Title. Location Salary Actions

GMP Inspector (Compliance )

Our client, based in Dublin city centre, requires a GMP Inspector to join their team. This is a 3 year Fixed Term Contract. Reporting to a Senior Inspector, the Inspector will be primarily responsible for assessing the compliance of manufacturers with EU Good Manufacturing Practice (GMP). The role of an Inspector is to evaluate the compliance of sites inspected, in Ireland & abroad, with the requirements of National legislation (in Ireland), European Community Directives, Regulations and Guidance. These sites may include; o Manufacturers & distribu...

Location: Dublin,
GMP Inspector (Compliance ) 		Dublin Not Disclosed

Quality/Commissioning Lead

Our client is an innovative organization who designs & manufacture clean room solutions for the Pharma & Biopharma industries. They have offices & manufacturing capabilities in both the US & Ireland. They are seeking a Quality Lead for their manufacturing in Kilkenny in Ireland. The successful person shall be involved in all inspection, testing, and commissioning activities throughout the product design, manufacturing and testing phases. The Quality lead will be responsible for following company procedures to ensure that our client provides a consistent...

Location: Kilkenny,
Quality/Commissioning Lead 		Kilkenny Not Disclosed

Director, Quality & Compliance (GCP)

Our client is a global Biopharma organisation who play a crucial role in developing life-saving therapies. They are seeking a Clinical Quality and Compliance Director who is ready to dive-in to support our clients clinical development programs. As a Clinical Quality and Compliance Director, you will support and work with our clinical study management teams and teammates across R&D Quality and Compliance. They need someone with strong leadership skills, expert Good Clinical Practice (GCP) knowledge, audit skills, communication, facilitation skills, and the ability to...

Location: Dublin,
Director, Quality & Compliance (GCP) 		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

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
Project Manager UDI Republic of Ireland Not Disclosed
Director of Quality Risk Management System Limerick Not Disclosed
Project Manager UDI Republic of Ireland Not Disclosed
Associate Quality Engineer Dublin Not Disclosed
Senior QA Assoicate Dublin Not Disclosed
Project Manager UDI Republic of Ireland Not Disclosed
GCP/Pharmacovigilance Inspector Dublin Not Disclosed
QA Specialist Limerick Not Disclosed
Project Manager UDI Republic of Ireland Not Disclosed
Project Manager UDI Republic of Ireland 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