Our client, a pharmaceutical service company based in Scotland, specialise in conducting research, development and manufacturing on a contract basis. This innovative company are currently looking for a Director of Quality to join their steriles division which manufactures investigational medicinal products.
As Quality Director you will have responsibility for the development of the site quality strategy and compliance with the site Quality Management System. You will liaise with the MHRA to maintain IMP MA, develop and manage the site validation master plan and manage the Quality Department, comprising QA, QC, analytical and microbiology.
The ideal candidate for this Director of Quality position will be fully qualified and accredited as a QP eligible for permanent provision in a steriles IMP MA, with considerable experience in a senior QA role within the pharmaceutical industry. Prior experience in sterile products manufacture is also essential.
This is a fantastic opportunity for an experienced Qualified Person to develop their career with a dynamic pharmaceutical service company who are committed to making a difference.
If you would like to hear more about this role, please contact Lorna Crombie on 01913848905 or email email@example.com, quoting reference DH19237 in all correspondence.
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