I'm looking for...

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
Contact Info
Jack Caffrey
Life Science

01 507 9279
[email protected]
Connect with me on
Program Manager
Quality Engineer
Regulatory Affairs Specialist
Republic of Ireland
Risk Manager
VP of R&D
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 [email protected]

QA Sr Associate

Reference:JSC00029968 Location: Dublin
Qualification:DegreeExperience:2-3 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Nurse Associate, QA Specialist

We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin.

This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

The Plant Quality Assurance (PQA) Snr Associate will typically report to a QA Manager and is a core member of the site Quality Assurance team.


  • Perform complaint investigation related to product manufactured including Formulation, Filling, Inspection and Packaging.
  • Perform all activities in compliance with Amgen safety standards and SOPs
  • Write, review and approve Standard Operating Procedures in accordance with Amgen Policies.
  • Provide Quality support for triage and investigation of Deviations
  • Review and approval of Deviations and CAPAs for closure ensuring compliance with appropriate documentation, whilst ensuring that CAPA actions address root cause and implementation plan dates are achievable
  • Review/approve production batch records, and associated documentation in preparation for Qualified Person disposition activities.
  • Review and approve cGMP records (e.g., deviations, CAPA, protocols, reports & SOP) ensuring compliance with appropriate documentation
  • Support continuous improvement and Operational Excellence initiatives
  • Any other tasks/projects assigned as per manager’s request.

Education & Experience

  • Experience with industry Investigating and complaints, Batch review.
  • Excellent written and verbal communication.
  • Experience working cross functional
  • Background, ideally within pharma either manufacturing, Quality, QC
  • Previous experience with batch review/investigations (min of 2 years’ experience) or willing to consider graduate at Masters or PhD level
  • Ideally some complaints handling
  • Experience working with dynamic cross-functional teams and proven abilities in decision making
  • Strong organizational skills, including ability to follow assignments through to completion
  • Demonstrated ability in problem solving and experience in managing Root Cause Analysis / Non Conformance /Deviation investigation
  • Knowledge of applicable Regulatory requirements, and ability to evaluate compliance issues
  • Operational Excellence experience
  • University degree. Engineering or Science related discipline preferred.

  • Relevant experience (2 yrs +) working in the pharmaceutical or biotechnology industry.