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Quality Assurance Auditor, Pathology Diagnostics Ltd., permanent
An exciting opportunity has become available within our friendly and enthusiastic team. Due to the growth of the organisation we are looking for a GCLP/GCP QA Auditor to manage operational QA activities related to clinical studies and to provide GCLP/GCP compliance support. In this position,you will lead the expansion and development of quality systems in a rapidly growing successful organisation.The successful candidate must have an extensive of knowledge of GCLP/GCP and the EU ClinicalTrials Directive along with the ability to manage GCLP quality systems. This role is a key positon within our organisation and it is essential that the candidate has the ability and dynamism to motivate organisational staff to achieve compliance as well a proven ability to manage relationships with representatives of external organisations including Sponsors and regulatory authorities.
Position requirements:A primary degree in science or other relevant speciality; A minimum of 5 years expertise in quality auditing for GLP/GCP preferably from working in a CRO or the pharmaceutical industry; extensive of knowledge of GCLP/GCP and demonstrated ability to apply this knowledge and effect organisational compliance; Prior experience of regulatory inspections with MHRA, HTA and other regulatory bodies; excellent interpersonal, communication and influencing skills; excellent organisation skills and ability to meet deadlines; ability to work in a team and be flexible.
Prior experience of histology laboratory technical activities is an advantage but not essential.
How to apply
To apply, please send a CV including qualifications and referees, plus covering letter to email@example.com.