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Quality Systems Specialist

Quality Systems Specialist

Duties and Responsibilities:

This role will be part of the QA Systems team based in a new state of the art single use multi-product biotech facility. The QA Systems Specialist will be responsible for supporting Site Quality Management Systems with responsibilities which may include; 

  • Supplier Quality Management activities

  • Change Management 

  • Document management 

  • Quality Approval of documents

  • Quality Oversight on pest control

  • Supporting Quality Council 

  • Inspection readiness activities 

  • This role will also support transition activities and integration to new quality management systems as required

Candidate Requirements:

Science or engineering Degree

Minimum of 4 years experience in a Pharma regulated environment in a similar role

Experience in change management, change control, documementation management and approval of Quality documentation

For a confidential discussion and more information on the role, please contact Rory Walsh.

Rory Walsh

087 126956