Job Title

QA Auditor - Cambridge

Salary

Day Rate/Negotiable

Job Type

Regulatory Affairs

Location

Cambridgeshire

Employment Type

Permanent Job

Employer Type

CRO Full Service

Seniority

Department Manager/Associate Director

Duration

 

FTE Hours

Full Time 35 - 40hrs Per Wk

Vacancy Status

Open For Applications

Date Posted

Mon 6th Oct 2008, 11:53am

Whilst your main audit activities will initially be project based, primarily performing site audits, you will also take part in system based audit programmes. As your career develops, and under the mentorship of a QA Manager, you will have opportunities to develop your skills and eventually have the ability to lead a wide range of audit activities. You will play a vital consulting and problem solving role for the clinical project teams. You will support client audits and regulatory inspections and contribute to PPD's ongoing quality improvement programmes.

You will need a passion for quality combined with excellent communication and interpersonal skills. You will be a life science graduate with experience in Quality Assurance and previous experience in clinical research (CRA, Project Manager or a related field).

All applicants will require a working knowledge of the background and application of GCP, basic business computer skills (MS Word, Excel, e-mail, etc) and a full driving license.