This expanding, global CRO ware looking to recruit a SrQA Auditor to join their offices in the UK.
In this role you will conduct all aspects of internal and external auditing, to include sponsor and investigator audits, to ICH GCP and ISO14155. Audits will be system, process, facility, documentation and site focused, across Europe. In addition to your auditing duties you will have the chance to get involved in supervising a junior QA Auditor, with a view to taking on line management responsibilities and a QA Manager role in the near future. This is an excellent opportunity to gain QA expertise within another area of clinical product development, whilst at the same time gaining valuable leadership and management skills for the future! Who are we looking for? A scientific background is essential along with a proven track record of auditing to ICH GCP requirements. The ideal candidate would have some exposure to device trials and auditing to ISO 14155 requirements. Full training will be provided to candidates with strong ICH GCP auditing experience looking for a move into devices. Practical experience with all types of internal and external audit is essential. A competitive salary and remuneration package is available to the successful candidate. If you are looking to broaden your auditing experience within clinical trials then please call Kristina on 01279 657716 or email Kristina@seltekconsultants.co.uk
Job Ref: 8103
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