he task: * Leadership and development of the improvement team * Recruiting, nurturing, developing and motivating the QA improvement team * Ensuring the timely processing of non-conformities and associated sub-processes * Responsible for production special releases "at risk" * Control/implementation of procedures in connection with quality assurance, "containment activities" on site
Your profile: * Completed studies (MBA, MSc., diploma, specialist) in the field of health, engineering, natural sciences or business administration or comparable qualification. * At least 3 years of professional experience in medical technology or an industry with a comparable regulated environment * Strong ability to lead people such as, ability to motivate, ability to work in a team and effective reporting * Communication skills, negotiation skills and assertiveness * Ideally, experience in the coordination, participation, implementation and follow-up of internal and, if necessary, external audits * Knowledge of ISO 13485 and 21 CFR Part 820, MDSAP and MDR standards
This global player provides you several careeru opportunities. If you are ready to make the next step, please send us your application.
