Quality Assurance Professionals

Dublin (City), Leinster (IE)
Negotiable depending on experience
23 Apr 2021
23 May 2021
Quality, GMP, QA / QC
Full Time
Contract Type
Experience Level
Experienced (non-manager)

My client, a global pharmaceutical company in the South Dublin area is currently recruiting for a Quality Assurance Professional to join their team.

The job

They are currently sourcing 3 QAP's to join a dynamic team that help improve our production processes. One position will be Permanent and the second will be Temporary (12-month) contract. Both positions will report to the Quality operations, Associate manager.

Working hours:

These roles will be a 16/5 shift role and the applicable shift rates will apply. There is also one temporary position that works from 9am-5:00pm


Key responsibilities would include (but are not limited to):

As a QAP you will have overall responsibility for the batch documentation review process in the company.

Lead and develop the team leaders in production towards a more LEAN and efficient way of working.

Work closely together with the QPs to ensure alignment on process/product investigations and follow up corrective actions.

  • To deliver efficient and timely review of Finished Product batch documentation for release and rejection activities.
  • To approve batch documentation
  • To approve the decision making on daily queries online and play an active role in the resolution of these issues.
  • To perform process confirmations on the production lines with regards to batch documentation and manufacturing.
  • To approve process/product investigations (deviations) and follow up corrective actions identified.
  • To approve temporary change requests.
  • To approve process/product investigations (deviations) and follow up corrective actions identified.
  • To support Customer complaint investigations and response where applicable.
  • To provide Quality inspections system support including action close-outs.
  • To update SOP/WI’s as required for the Quality Release Department.
  • ·To complete approval of Quality Management System records, CAPA’s, actions etc

What you need to succeed:

  • A minimum of an honours degree in Chemistry, Biology, Engineering or equivalent third level degree qualification.
  • At least three years’ experience in a quality or manufacturing function within the pharmaceutical industry.
  • Strong understanding of pharmaceutical quality processes and systems, manufacturing processes and other support/control systems is desirable.

Behaviours & competencies:

· Employee routinely will lead activities, initiatives or projects key to the delivery of a department’s overall objectives.

· Handles unfamiliar situations and solves problems to deliver results. Works independently and will typically supervise / instruct other professionals.

The deadline for applications will be 04/05/2021


For a full Job Spec and to apply for this role please call Zoe on +353 1 2784671 or e-mail zhamilton@thornshaw.com

Thornshaw Scientific Recruitment is a leading Irish provider of specialist Scientific Recruitment. Part of the CPL Group. www.thornshaw.com Tel: +353 1 2784671

Apply for Quality Assurance Professionals

Already uploaded your CV? Sign in to apply instantly


Upload from your computer

Or import from cloud storage

Your CV must be a .doc, .pdf, .docx, .rtf, and no bigger than 1MB

4000 characters left

Marketing Communication

We'd love to send you information about Jobs and Services from PharmiWeb.jobs by email.

All emails will contain a link in the footer to enable you to unsubscribe at any time.

When you apply for a job we will send your application to the named recruiter, who may contact you. By applying for a job listed on PharmiWeb.jobs you agree to our terms and conditions and privacy policy. You should never be required to provide bank account details. If you are, please email us.

Similar jobs

Similar jobs