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Search Results for Quality Auditor
Job Title. Location Salary Actions

GMP Inspector

GMP Inspector Reporting to a GMP Inspection Manager, the GMP Inspector will be responsible for assessing the compliance of manufacturers with EU Good Manufacturing Practice (GMP). The Manufacturing Compliance Specialist will evaluate the compliance of sites inspected, in Ireland and abroad, with the requirements of National legislation European Community Directives, Regulations and Guidance. These sites may include; • Manufacturers and distributors of medicinal products. • Manufacturers of investigational medicinal products. • Sites involved in ...

Location: Dublin,
GMP Inspector 		Dublin 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
Other Quality Assurance Jobs
Job Title Location Salary Actions
QA Specialist Cork Not Disclosed
QA Specialist Cork Not Disclosed
QA Specialist Cork Not Disclosed
Director, Pharmacovigilance Quality & Compliance (GVP) Dublin Not Disclosed
Associate Manager (Technical Training) Limerick Not Disclosed
QA Specialist Cork 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