Description
Responsibilities:To perform the duties of a QP in compliance with all applicable EU GMP regulations and directives.
To facilitate Quality management and lead the development of good quality culture.
Batch assessment and release activities to ensure compliance and efficiency and to meet regulatory standards.
Requirements:
7+ years experience of sterile manufacturing experience is mandatory.
Life Sciences Degree Eligible as a QP.
Relevant experience within a Pharmaceutical Quality Assurance / GMP background.
Knowledge of process improvement techniques an advantage.
Detailed knowledge of GMP requirements for product manufacturing, packaging, licensing, release and post-market responsibilities.
If you are interested in this position please contact Sarah Irvine on or reply with a copy of your up to date CV. We also offer shopping vouchers for any successful referrals so if you know of anyone who may be looking please get in touch.