You will act as Qualified Person (QP) for all products manufactured on the site and will be the key contact point for all QA/GMP issues on the site. This is a permanent position.
As a QP you will be responsible for the release of products to the market within the Directive 2001/83/EC and as named on the Manufacturer’s Licence. You will also release both Raw Materials and Bulk products and act as deputy Pharmacovigilance Qualified Person.
As part of this QP role you will be expected to develop appropriate QA systems for the site, approve master batch manufacturing and packing documents, review and QA approve SOPs, manage and implement the internal and external audit programmes and to review and approve change requests.
The ideal candidate for this QP role, you will hold a chemistry or pharmacy degree (or equivalent), will be on the register of eligible Qualified Persons and named in the appropriate Manufacturer’s Licence. You will also have experience gained within the pharmaceutical industry of working in a laboratory and an appreciation of other aspects of the business.
For more details, or to apply for this Qualified Person position, please contact Jason Johal at CK Science on 01438 723 500 or email firstname.lastname@example.org. Please quote reference ST20451 in all correspondence.
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