Description
Responsibilities include:To lead batch assessment and release activities ensuring releases are carried out efficiently, in a timely manner, and meeting relevant regulatory standards.
Performing duties of the Qualified Person in compliance with all applicable EU GMP regulations and directives.
Improving quality, facilitate Quality management and leading the development of a right first time, quality culture.
Minimum requirements:
5+ years experience Previous Sterile Manufacturing experience is mandatory.
Life Sciences Degree and must be eligible as a QP.
Relevant experience within a Pharmaceutical Quality Assurance / GMP background.
This is a fantastic opportunity to join a fast paced environment working alongside an expanding team. If you would like to know more about this opportunity please contact Sarah Irvine on or reply with an up to date CV.
We also offer shopping vouchers for any successful referrals so if you know of anyone who may be suitable for this position please feel free to get in touch.