CQV Specialist (Commissioning & Qualification)

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. Their strategic priorities are to drive optimum performance of their existing products, enabling access for patients today and building their pipeline through research and development to deliver patient access in the future. 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 Global External Supply group for an experienced CQV Specialist to join this company.

The Position

With a direct line of report into the CQV Lead on site and supported by the team in Dublin, you will be responsible for ensuring that the manufacturing facility, utilities and systems are qualified to meet corporate and regulatory requirements. As CQV Specialist you will co-ordinate, review and support the execution of validation activities.

The Person

You must possess the following in order to qualify:

  • A Bachelor’s degree in a Science or Engineering related discipline
  • Minimum of 7 years’ Validation industry experience working in a GMP or cGMP regulated environment – Pharmaceutical / Medical Device / Biotechnology preferred
  • Proven track record of working as a CQV or Validation Engineer
  • Must be able to analyse data using basic statistical methods
  • 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: On Application Location: Dublin West