For our client, a Swiss BioTech company based in Zurich, we are looking for a committed Quality Assurance Manager. The company has successfully established itself in the Swiss market and worldwide. In this role, you will be directly reporting to the senior management.
Your tasks:Managing and developing Quality Management System according to ISO 13485Monitoring quality indicators and quality improvement measurementsInterpreting and implementing GCP/GMP guidelinesManaging CAPAs system and root cause analysisCoordinating qualifications and validations processesCoordinating international project teams and regulatory projectsResponsibility for the compliance with regulatory and quality provisions and guidelines
Your profile: Degree in sciences, engineering or similar formulationProfessional experience in Quality Assurance, SOPs, GMP/GDP, GCLP, GMP, IMPs, GxP vendors (e.g. CMOs)Minimun three years of work experience in a GCP compilance role Over five years of professional experience in quality assurance in the medical device industryProficient regulatory knowledge for Switzerland as well as EUFluent German and English Excellent communicative skillsInnovative and analytical thinkingIndependent way of working
Are you willing to join a global operating company? To engage in the recruitment process, please submit your CV via the apply button. In case you have any questions, please do not hesitate to call me during CET office hours.
Dr. sc. Sanja Centineo
Industry & Manufacturing