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.
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.
You must possess the following in order to qualify:
To find out more apply online or call Gillian McMurrough directly on +353 1 6321827 for a confidential discussion.