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

Associate Director Quality Systems

Reference:SCAXHY-583326 Location: Limerick
Qualification:DegreeExperience:7-9 Years
Job Type:PermanentSalary: Not Disclosed

Associate Director Quality Systems
Our client, a leading biotech organisation are currently recruiting for an Associate Director Quality Systems to join their team on a permanent basis. As Associate Director Quality Systems you will provide broad Quality Assurance expertise and leadership as required with an understanding of local regulatory as well as global expectations. You will be the Site Owner of a number of Quality Systems and responsible for identifying potential risks within the systems and communicating/collaborating with other functions.


  • Ensure the Quality Systems adhere to tight internal standard and including the Local / International regulatory bodies
  • Identify leading practices and recommend improvements to continuously improve compliance profile
  • Identify Trends in recent regulatory inspections and translate this to recommendations to enhance readiness
  • Work closely with other compliance teams to close gaps, improve practices and maintain compliance
  • Define and implement quality standards, systems and metrics for maintaining regulatory compliance for operations
  • Interface with Customers/partner quality organisations as required
  • Participates on internal committees/teams as required
  • Provides advice and direction to other company departments on quality issues
  • Provide support during inspections and audits


  • Honours Degree BS/BA in Life sciences or B. Eng. in Mechanical or Biomedical engineering (or equivalent), Master’s degree a plus
  • Min 8+ years of relevant progressive experience in QA within the Pharma / Biopharma Industry and some experience working with Global Regulatory Agencies
  • Proven experience leading teams in achieving company goals