Document Control Specialist – Quality Assurance

One of the world’s leading speciality pharmaceutical companies are expanding their operations in Ireland. Through acquisitions and mergers, this company has expanded rapidly in its short history and now boasts more than 10,000 employees, and offices in more than 40 countries worldwide. Operating two state of the art GMP facilities in Dublin with virtual management of CMO operations on site also, a new role has been created within the Quality Assurance Compliance group for a Document Control Specialist to join this company.

The Position

With a direct line of report into the QA Compliance Manager, as Document Control Specialist you will be responsible for performing document control processes to ensure that controlled documents are revised, approved, distributed, and archived using Master Control. Controlled documents include policies, standard operating procedures, work instructions, forms, protocols, reports. You will additionally support the associated Compliance Wire training system across the site.

The Person

You must possess the following in order to qualify:

  • A Bachelor’s degree in a Science or Engineering related discipline
  • 1-3 years direct pharmaceutical, medical device, or biotechnology experience, preferably in quality or regulatory affairs role in a GMP or cGMP regulated environment
  • Proven document control experience
  • Team player and willing to work in a changeable, busy environment and work cross functionally with various teams within Quality
  • Hold an EU passport or be eligible to work within the EU

To find out more apply online or call Gillian McMurrough directly on +353 1 6321827 for a confidential discussion.

Salary: €35000 - €38000 Location: Dublin West