Job Opportunity

Reference: QS0985
Title: Qualified Person (QP) Manager
Location: Norfolk
Job Type: Full time permanent
Salary: £70,000 - £85,000 per annum
Contact Person: Miss Selina Thompson apply@qualitystart.co.uk

Opportunity: This is a fantastic opportunity for a Qualified Person (QP) to join a global pharmaceutical manufacturing company based in Norfolk.

Your role as a QP will involve:

• Timely release of all drug products, medical devices and unlicensed drug products.
• Ensuring suitable contracts and technical agreements are prepared and implemented relating to the manufacture, packaging, testing and distribution of medicinal products.
• Notifying senior management of any issues related to GMP, product quality and any other matter that requires their attention.
• Participating/leading in the review of any complaint, deviation investigation, or product recall.
• Providing support to the auditing of contractors and key suppliers against Marketing Authorisations and relevant GxPs.
• Inspecting contractors' facilities and production documentation at intervals to establish and maintain working relationships with people in positions of responsibility and maintain confidence in their application of GxP and requirements of Marketing Authorisations.
• Reviewing and approving SOP's and other relevant GMP documents relating to the manufacture, labelling and assembly operation, storage, distribution and QC testing of drug products.
• Support the implementation of the Global Quality Directives.

This is a full time permanent job opportunity based in Norfolk paying an excellent salary of £70,000 - £85,000 per annum and great benefits such as 25 days holiday plus bank holidays on top, Pension, Life insurance, Childcare vouchers and much more.

Skills:  To apply for the role of Qualified Person you will have the following:

• A degree in one of the following scientific disciplines: Pharmacy, Medicine, Veterinary Medicine, Chemistry, Pharmaceutical Chemistry and Technology, Biology.
• Experience working as a QP which ideally will involve prior experience in the certification of sterile dosage forms (either terminally sterile or aseptic) – flexible on this.

How to Apply: In order to apply for this vacancy please ensure you have read and agree to the privacy policy found here and then email your CV to apply@qualitystart.co.uk quoting the reference number and the job title.