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.
The role will require working on-site for five days a week and is offering competitive daily rates.
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.