Description
Key Responsibilities:Leading batch assessment and release activities to ensure releases are carried out efficiently, in a timely manner, and meeting relevant regulatory standards.
To perform all Qualified Person responsibilities in line with all cGMP regulations.
To improve quality on a daily basis and to develop the Quality culture within the site.
Minimum requirements Education:
7+ years experience within the Quality function in Pharmaceuticals.
Life Sciences Degree Eligible as a QP.
Detailed knowledge of GMP requirements for product manufacturing, packaging, licensing, release and post-market responsibilities.
Good level of use of Lotus Notes, Excel, and Word.
Good communication skills.
Pharmacy Qualification would be beneficial.
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.