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

QA Specialist

Reference:BCACIS-656857 Location: Cork
Qualification:DegreeExperience:3-4 Years
Job Type:PermanentSalary: Not Disclosed

Our client in Cork, a leading pharma company, are seeking an experienced QA specialist. This individual will contribute to the implementation and maintenance of Quality Assurance actions in compliance with the current GMP regulations.

With primary responsibility for the quality assurance in Operations and Manufacturing and the relevant supporting departments such as Laboratory, Validation, Engineering and Warehouse.


Product release activities
Review all documentation associated with batch release to ensure GMP compliance.
Ensure the follow-up of the necessary corrective actions & preventative actions implemented in consequence of a quality failure
Perform investigations, and ensuring a follow-up, following discrepancy, failures and external complaints.
Participate in KPI meetings to assist the batch release process.
Implementation, maintenance and development of QA systems.
Write and review QA department procedures and reports eg. protocols, SOPs , environmental reports etc.
Carry out the inspection, investigation, and taking of samples where appropriate, in order to monitor factors which may affect product quality.
Alert the QP in case of detection of a discrepancy anomaly or GMP practices discrepancy / non compliances
Participate in management and administration of change control activities on site.

Education & Training Educated to third level in science based discipline.
Degree level preferable.
Experience Minimum 3 years pharmaceutical experience in a regulated environment would be preferable. Experience in pharmaceutical environment a significant advantage.
Competencies Knowledge of GMP. Good organisation skills and time management. Analytical approach to problem solving.

Contact Brian Christensen on 01 6854747 or submit your CV to for immediate consideration
If you would like further Information you can contact the recruiter directly:

Brian Christensen | Tel: +353 (0) 1 685 4747