Job Description:
In this role you will plan and conduct audit programs, prepare reports to verify regulatory compliance. This includes define and implement quality indicators for qualitative and quantitative evaluation, provide operational support for internal quality. This role requires at least 3-5 years experience in related role, strong clinical trial experience, a good knowledge of ICH-GCP and compliance. French and English language knowledge is required. This role is a very good stepping stone to further develop your skills within a well-organized company according to your chosen career path. In the meantime the helpful colleagues can make your job really exceptional. The company offers competitive salary. To find out more, send your CV in Word format to a.kocsis@nonstop-recruitment.com or call NonStop Pharma Recruitment on +44 203 519 1775 and ask for Anita Kocsis.