Description
The ideal candidate will have an opportunity to join a dynamic and fast moving organisation to focus on:Leading batch assessment and release activities to ensure 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 Education:
5+ years experience
Previous Sterile Manufacturing experience is mandatory.
Life Sciences Degree Eligible as a QP.
Relevant experience within a Pharmaceutical Quality Assurance / GMP background.
Experience within the Pharmaceutical Industry.
Knowledge of process improvement techniques an advantage. Pharmacy Qualification would be beneficial.
Detailed knowledge of GMP requirements for product manufacturing, packaging, licensing, release and post-market responsibilities.
Good working knowledge of problem solving and evaluation techniques.
Good level of skills in the use of computer based systems, this is to include Lotus Notes, Excel, and Word.
Good communication skills to ensure information is taken, used and given at all levels for maximum benefit to the business.
Please contact Sarah Irvine on if you are interested in this position or reply with a copy of your most recent CV. We also offer shopping vouchers for any successful referrals.