The Client
My client is one of Irelands largest pharmaceutical manufacturers. Based in Co Down, but with locations globally. A vacancy has arisen for a QA Validation Specialist to join their Quality function.
The Role
Based within the QA Validation Department, the successful candidate will be involved in the QA review of computer systems validation lifecycle documents. The successful candidate will support the QA Manager in ensuring that all regulated computer systems in use are identified, evaluated, validated, maintained and periodically assessed in accordance with cGMP and company procedures.
The Person
· Third level qualification in a scientific, information technology or engineering discipline.
· At least two years’ experience in a computer systems validation or equipment qualification or similar QA role.
· Good working knowledge of current Good Manufacturing Practices (cGMP) and current Good Laboratory Practices (cGLP).
To discuss this on any other role in Life Sciences, call Seamus on 02890725625
