As the premier, independent, UK-based provider of bioanalytical services to the world's pharmaceutical industry, we have strong ideas about the value of our staff in providing a top quality, scientific service to our clients. We recognise that it is important to provide an environment in which our employees feel valued and are able to develop to the best of their abilities. This is complemented by a truly competitive salary.

We require the following individual to join our friendly, professional team at our regulated site in York:

The successful candidate will undertake independent Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) monitoring of work conducted in the company’s bioanalytical laboratory facilities as required by regulatory guidelines.

The ideal candidate will have:

• Experience of working within a GLP/GCP compliant environment
• Understanding and knowledge of GLP/GCP/Good Clinical Laboratory Practice (GCLP) quality assurance requirements

• Capability to perform independent audits
• Good verbal and written communication skills
• Practical knowledge of carrying out GLP/GCP audits
• General awareness of industry quality systems/ standards

• Ability to work in a team environment

• Flexible approach to their work
• Meticulous attention to detail

Candidates will ideally be educated to degree level, preferably in a relevant scientific subject and have a minimum of three years’ experience within GLP/GCP/GCLP Quality Assurance or at least three years’ experience within a GLP/GCP/GCLP environment or equivalent experience working within an organisation supported by a quality management system. Experience in the field of bioanalysis would be considered highly advantageous.

The grading of this role is flexible dependant on experience and relevant qualifications.