Quality Director - Speciality Pharmaceutical Company

Recruiter
Skills Alliance Limited
Location
Cardiff (Caerdydd)
Salary
£70000 to £95000
Posted
13 Nov 2017
Closes
16 Nov 2017
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Quality Director - European Speciality Pharmaceutical Company - South Wales, UK

Skills Alliance have partnered with a multi-faceted European speciality pharmaceutical company for the appointment of a Quality Director responsible for quality and regulatory compliance on a large, fast-paced manufacturing site as well as ensuring all products are manufactured in line with internal and external regulatory requirements.

Company Overview

Well-established, European-based speciality pharmaceutical organisation that are renowned for their agile, pragmatic partnerships with some of the industry's leading Biotech/Pharmaceutical companies. Multiple sites across the EU that develop and manufacture a broad portfolio of medicinal products and medical devices. Strong reputation for organisational Quality and boasts a talented, well-established Quality department.

Role Overview

As Quality Director your remit is broad and far-reaching, transcending the Quality Department and influencing almost every function within the business to drive Continuous Improvement initiatives in order to achieve excellence. As part of the Site Leadership Team you will be repsonsible for the management of the Site Quality department including operational Quality oversight; responsibility for ensuring compliance to relevant regulatory requirements (GMP, ISO 13485 etc) and internal standards and designing and managing the departmental budget. You will also be an influential figure in the Global Quality organisation; responsible for company-wide Quality Strategy design, implementation and drive.

Experience Sought

Eligibility to and experience of acting as a Qualified Person under Directive 2001/83/EC and 2001/20/EC and an RP (on a WDA) is essential, as is significant experience in a Quality leadership role (Senior QA Manager, Head of Quality, Quality Director etc) within the manufacture of medicinal products and medical devices. Thus, thorough knowledge and application of cGMP, GSOP and ISO 13485 is essential. Demonstrable experience of designing and managing departmental budgets is also critical in the success of this role.

If you would like to be considered for this opportunity, please click APPLY to send a copy of your CV. For further details and a full job description, please call Joshua Godden on Phone number removed or e-mail Joshua.Godden @SkillsAlliance.com. All inquiries are treated confidentially.