Qualified Person

Challenging and Rewarding Career Opportunity for a QP who will Report Directly to the Head of Quality and will Work with Other QPs, Including Contract QPs and Site Management, Ensure the Local and Global Quality System Operates in Accordance with GMP

ROLE

The QP will Undertake Duties Specified in

• EU Directive 2001/83/EC as Amended (Medicinal Products for Human Use)
• 2001/20/EC (IMP Products)
• 2003/94/EC Principles and Guidelines of GMP for Medicinal Products for Human Use
• 2011/62/EC Falsified Medicines Directive, QP Code of Practice for Qualified Persons involved in the manufacture of pharmaceuticals,
• Eudralex Volume 4 Annex 16

The QP will also

• Review, Certification and Release of Batches
• Act as QA Site Lead

REQUIRED

• Eligible to be Nominated as a Qualified Person on the Manufacturing Licences
• Member of a Relevant Professional Bodies to Permit QP Eligibility
• Previous Experience in QP Certification of Medicinal Products
• Previous Experience in a Pharmaceutical Manufacturing Organisation, Ideally with Sterile Products

REMUNERATION

• £85K with Bonus and Excellent Benefits Package

RESPOND

• Call Luke Blaney on +44 (0)1580 211221 to Learn More about this Career Opportunity or e-Mail luke@arxconsultancy.com with Your Application, Including Your Current CV