Closing Date 9 Aug 2010
Location Tredegar, Gwent, South Wales

Salary:

TBA

This role will assist the Quality Director in ensuring that all activities are in compliance with Good Manufacturing Practice and work closely with Manufacturing, CTS, Development, Engineering and Quality Control Departments to provide control of documentation as well as QA review of laboratory activities and associated data.

The ideal candidate will be educated to degree level and be a member of a professional body as recognised by the UK MHRA or be progressing towards such membership and ideally six years plus experience within the pharmaceutical industry with a diverse knowledge of various dosage form manufacturing. Good written and verbal communication skills are essential to this role along with excellent analytical problem solving abilities.

If you are interested in applying, please complete an application form and foward it to Anne.Trehearne@pennpharm.com or post it to HR Dept., Penn Pharma, 23-24 Tafarnaubach Industrial Estate, Tredegar, Gwent NP22 3AA.

• Penn Employment Application Form (1248k)