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An exceptional opportunity has arisen for a Quality Assurance professional and Qualified Person to join a world leading Pharmaceutical company who work in one of the most exciting areas of modern medicine based in Kent in the South East of England as a Quality Assurance (QA) Manager and Qualified Person (QP).
This expanding and highly successful research and development company manufactures Pharmaceutical prescription products in an extensive range of therapeutic areas including oncology, epilepsy and inflammation. This innovative Pharmaceutical Company are at a key point in their development with large scale Phase III studies currently running with high prospects.
As the Quality Assurance (QA) Manager & QP you will report directly to the site Head of Quality as well as manage the GMP QA group and QMS along with having the following responsibilities:
Support the growing, extracting and manufacture of drug substances and drug products derived from botanical materials,
Utilise your GMP knowledge and leadership skills to oversee the compliance programme for the company's manufacturing and development function,
Manage key performance indicators,
Oversee the audit programme including internal systems, external suppliers, documentation and contractor audits,
Provide support, advice and training to other departments,
Provide assistance when required with cross-functional GCP, CSV and GLP audits.
The role will require you to have a minimum of 5 years management experience as well as be eligible to be named on both the MIA and MIA (IMPs - investigational medicinal products) licences. Furthermore, you should have direct experience in practicing as a QP in the release of both commercial products and investigational medicinal products (IMPs) for solid and liquid dose forms. You will also have a working knowledge of FDA GMP requirements and excellent communication and leadership skills.
This is a unique and exciting opportunity to work within an exception career driven and progressive Company working in a broad based position, providing exposure to all aspects of drug development and offering excellent benefits including competitive salaries, a pension scheme, performance related bonus, health insurance and a generous holiday entitlement.
Key Words - QA, Quality Assurance, Qualified Person, QP, IMPs, Ivestigational Medicinal Products, MIA, FDA, audit, solid, liquid, Manager, QA Manager, GMP, good manufacturing practice, Kent, South East, England, UK
For further information on the role or company please contact myself, Sara Cork at Paramount Recruitment on 0121 616 3464.Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.