Our client is one of the world's leading biopharmaceutical companies who operate a state of the art manufacturing facility in Dublin. They seek to hire an experienced QA professional (QP) for a 12 month fixed term contract. The role will be based at their manufacturing facility and will work within the disposition team supporting manufacturing onsite for Global supply.

The Role:

The QA Specialist (QP) will report to the Senior QA Manager and act as an SME within the Quality group. The position sits at a manager level within my client's organisational structure.

Key objectives:

• Routine QA duties to support manufacturing pf product for global supply.
• Oversight and responsibilities for key quality systems and processes.
• To act as a key quality reviewer and approver on GMP documentation.

The Person:

In order to be considered you must have the following:

• A third level degree in Science, Engineering or related.
• Must satisfy requirements outlined in Directive 2001/83/EC to be eligible to act as a QP.
• 4-8 years industry experience within the Pharmaceutical or Biotechnology sectors.
• Strong communication skills and an ability to influence key stakeholders.
• Eligibility to work in the EU.

To discover more about this opportunity, apply now or contact Gillian McMurrough at HRM on +353 1 6321827 for a confidential discussion.