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

Salary:

TBA

This role will be responsible for the timely review, completion and approval of technical and quality documentation in compliance with GMP and other industry regulations and assist in assuring the Quality Management System is kept up to date in relation to general requirements. Candidates should be educated to degree level in a science discipline with a minimum of 5 years experience in a regulated pharmaceutical environment.

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)