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

Salary:

TBA

This role is primarily a technical role with the responsibility to assess and perform GMP requirements. Key responsibilities include providing expert advice on clinical trial projects, review and approval of technical and quality documentation. Candidates should have as a minimum BTEC Pharmacy with 3 years experience in a regulated pharmaceutical environment within clinical trials. Knowledge of GMP, GCLP and GCP regulations and international requirements are essential, along with excellent problem solving skills and computer literacy.

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)