Your new roleAs Quality Manager your responsibilities will include:Design, implement and manage QMS ensuring full compliance for UKAS ISO17025, lead, plan & schedule all routine internal/ external audits. You will have ownership and management of all Quality non-conformances identified during internal and external audits and customer complaints. You will conduct root cause analysis, monitor nonconformities and strive for continuous improvement in all processes/ workflows relating to Quality Assurance. What you'll need to succeedIdeally you will be qualified to degree level in Biomedical Sciences, Biochemistry or a Life Science. Significant experience of operating within ISO Quality Management Systems of clinical operational laboratory environments. Experience in conducting audits and hosting external auditors.Experience working within a laboratory setting working to relevant ISO accreditation standards; ISO 17025. You will be highly motivated, independent and proactive and have a strong work ethic. Manage multiple priorities and adapt to change in a fast paced environmentWhat you'll get in returnCompetitive salaryCareer progressionPensionHealthcareFree parking
Possible hybrid working on occasionWhat you need to do nowIf you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.