Junior Regulatory Affairs Specialist

vor 3 Wochen


Bülach, Schweiz Teleflex Incorporated Vollzeit

About Teleflex IncorporatedAs a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.Position SummaryThis role will be located at the Bulach, Switzerland location which is responsible for the development, production and marketing of balloon catheters and drug-coated stent systems.We are seeking a new team member for our Vascular Intervention (VI) regulatory affairs group. The regulatory affairs department is responsible for worldwide registration of the newly developed class II and III innovative products and the existing portfolio.Principal ResponsibilitiesSupporting product registrations in low-effort countriesMaintaining the project status of registrations in the regulatory database, change projects overview and documentation overviewSupporting the worldwide assessment of changesMaintaining regulatory documentation up to date for global registrationsAssessing and clarifying the requirements for new Vascular Intervention device registrations and the regulatory impact of changes in assigned low-effort countriesStaying up to date with the latest regulatory requirements in assigned countriesEducation / Experience RequirementsUniversity degree in natural sciences, pharmacy, pharmacology, medicine or engineeringOne year of experience with registrations of medical devices is a plusLiterate in Microsoft Office and Adobe applications; SAP knowledge is an advantageAbility to work in a team, attention to detail, analytical skills, excellent organizational skills and ability to work on multiple projects with tight timelinesAbility to adapt to program/timeline changes as neededFluency in English is mandatory; German and any additional language are an advantageTeleflex is an equal opportunity employer. Applicants will be considered without regard to age, gender, race, nationality, ethnicity, civil status, family status, sexual orientation, disability, religion and/or membership of the traveller community.If you require accommodation and support to apply for a position, please contact us at talent.emea@teleflex.comDiversity fosters innovative thinking and entrepreneurship and that’s what we are about at Teleflex. We trust and value our people and their diversity and we make it fun to work here. We are on a journey to ensure our workplaces mirror the patients we serve and the communities we operate in. Our approach is simple, we embrace everyone and want them to feel they belong here. We are building a culture where all employees can bring their best and unique selves to work. If that appeals to you, we would love to hear from you. Come join a company where diversity is sought out and inclusivity is how we progress. #J-18808-Ljbffr



  • Bülach, Schweiz Teleflex Vollzeit

    About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology...


  • Bülach, Schweiz Teleflex Incorporated Vollzeit

    A global provider of medical technologies seeks a dedicated team member for regulatory affairs to assist in product registration and maintain documentation for innovative vascular intervention devices. This role requires a university degree in a relevant field, teamwork, analytical skills, and fluency in English, with proficiency in German being a plus....


  • Bülach, Schweiz BIOTRONIK Vollzeit

    Legal Counsel BIOTRONIK is one of the leading manufacturers of cardio - and endovascular implants and catheters for cardiac rhythm management, electrophysiology and vascular intervention. As a globally active company headquartered in Berlin, Germany, we develop, produce and distribute high-quality medical products based on the latest technology and...