Description
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:
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.
Solid dose experience is also essential.
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 Rachel Smith on if you are interested in this position or if you know anyone who may be suitable.
To find out more about Real please visit www.realstaffing.com