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 Senior Validation Analyst within their validation team
The Role
The successful candidate will be responsible for scheduling, supervising and executing all aspects of cleaning validation studies, including collection and analysis of cleaning validation samples and completion of all associated documentation in accordance with the relevant validation protocols, validation master plans and standard operating procedures. The successful candidate will also, where necessary, support completion of all other functions of the Validations Team.
The Person
· Third level qualification in a chemistry related
· Two years’ experience of working in a laboratory in the pharmaceutical industry or similar regulated environment.
· Good working knowledge of current Good Manufacturing Practices (cGMP) and current Good Laboratory Practices (cGLP).
· Extensive practical knowledge of HPLC analysis.
· Excellent protocol and report writing skills.
To apply for this role contact Seamus on 02890725625, or send your cv using the link provided