Forgot your Password?
Find this page useful? Click

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

Google Chrome
Internet Explorer
Mozilla Firefox

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Apply for this job






Salary Expectations:



Current Location:

Notice Period:

Write here your cover note:

If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to

Qualified Person (QP)

Reference:SCAXHK-554022 Location: Galway
Qualification:DegreeExperience:3-4 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Qualified Person

Qualified Person (QP)
Our client a global healthcare organisation, are currently recruiting for a Qualified Person to join their team on a permanent basis.


  • Perform QA/QP batch release as required to support operational business requirements (you will be required to be named on the site manufacturing licence as a QP and perform QP batch release as per current relevant EU guidelines)
  • Provide technical expertise for all QA and compliance topics/issues as required
  • Provide QA input into relevant Risk Management programmes within the company and to utilise risk management tools to support science based decision making in support of the highest product quality, safety and efficacy standards
  • Assist with development and implementation of effective performance monitoring indicators for the Quality Assurance department
  • Perform timely review of documentation/investigations/reports highlighting and assisting in the resolution of issues commensurate with the level of risk
  • Provide support for deviation investigations, including root cause analysis and corrective and preventative action (CAPAs) proposals and initiatives
  • Ensure relevant QA documents and procedures are approved to schedule to support technology (external and internal) transfers and new product introductions
  • Actively contributes to continuous improvement activities
  • Minimum of a Bachelor’s degree in a Science related discipline with a minimum of 5 years’ relevant experience within the Pharma industry or a related field.
  • Must be eligible for Qualified Persons status as per EU guidelines
  • Previous experience in a sterile product manufacturing facility is highly desirable
  • Quality system aspects experience including: Deviation management, CAPA, complaint handling, auditing, change management, supplier qualification, and batch release is desirable
  • Working management of risk management tools (eg. Hazard Analysis and Critical Control Points and / or Failure Mode Effect Analysis
  • Ability to handle multiple tasks in a fast-paced environment with strong organisational and time management skills
  • Must possess very good verbal and written communication skills, presentation skills, organizational skills and IT systems and software packages with strong working knowledge of Microsoft Office (Word, Excel, PowerPoint, etc.)
  • Self-driven attitude, demonstration of curiosity and innovation to drive project development forward