Job Title: Clinical Quality Assurance, QA Senior Specialist – IVDs/DevicesJob Type: Full time, permanent positionRemuneration: Up to £41,000 OR €47,000 + 8% bonus + benefitsLocation: Manchester, UK OR Barcelona, Spain (hybrid)Position DescriptionAn exciting new role has arisen within the Quality Assurance team. Based at either our Barcelona or Manchester sites, the successful candidate will take on responsibility for quality and compliance oversight of the activities performed by the Clinical Affairs team, in support of the testing and registration of diagnostic tests covering a diverse portfolio of indications. The scope of the trials is global and includes multi-centre trials managed out of several different locations.Key responsibilities:Work with members of the Clinical Affairs team to ensure compliance during trial activities – e.g. closure of deviations, complaints etc.Represent Clinical QA as a member of project teams for planned and ongoing clinical trials, including Quality review of clinical relevant documentationSupport qualification and perform independent QA audits of clinical study sitesParticipate in the internal audit programReview Clinical Affairs SOPsPosition RequirementsDegree qualification in a relevant subject, or equivalent employment experienceProven working experience as a Clinical Research Associate or similar with knowledge of relevant regulations, standards, guidelines and best practiceDesirable: working knowledge of In Vitro Diagnostic or Medical Device RegulationsDesirable: experience as an Auditor and/or Subject Matter Expert in regulatory inspectionsWillingness and availability to travel internationally (Europe + USA) up to 10%Ability to work independently while exercising good judgement and decision making within defined practices and policiesExcellent communication and interpersonal skills with the ability to work effectively with multinational/ cultural teams and individualsFor more information, please reach out to me at lucy.kirkaldy@cpl.com