Date: Aug 4, 2026
Location: Bülach, ZH, CH
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Company: Teleflex
Expected Travel: None
Requisition ID: 14203
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 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 Summary
The Medical Affairs Group with Teleflex in Bülach, Zürich is responsible for the design, conduction and evaluation of international first-in-men, regulatory submission and post-marketing trials as well as investigator-initiated trials. The Safety Group is responsible for the review, assessment, and reporting of adverse events from clinical trials to European and international Competent Authorities and Ethics Committees according to their specific requirements.
Principal Responsibilities
Assuring compliance with applicable standard operating procedures, work instructions, guidelines and regulatations
Managing adverse events/ device deficiencies from recording in electronic case report form (eCRF) until completion
Assuring compliance and adherence to adverse event reporting requirements
Authoring periodic safety reports to authorities, relevant sections in clinical investigation plan, and data monitoring committee charter
Collaborating with clinical data operations team, clinical project management team, and monitors
Initiating, managing, monitoring collaboration with Contract Research Organizations / Consultants
Representing the Clinical Safety & HEOR Team in assigned (study) core team meetings, and meetings with Medical Affairs and within the company
Training of internal and external study team members
Ensuring compliance with corporate values
Education / Experience Requirements
University degree or equivalent in medical sector. Alternatively medical background (e.g., nurse, cath-lab technician)
Previous experience as a Safety Officer, Clinical Safety Specialist, or in medical device safety/pharmacovigilance is highly desirable and will be considered an advantage
Team player with strong people skills: Verbal communication, listening, proactive, conflict resolution, diplomacy, decision making and collaboration
Personal skillset ideally includes strong troubleshooting, organisation/planning & time management, service orientation, work ethics, taking ownership, attention to detail
Understanding of ISO 14155:2020/2024, Medical Device Regulation (MDR, 2017/745) and Medical Device Coordination Group 2020-10/1 requirements
Language skills: English, fluent both written and spoken; German, basic understanding both written and spoken
Computer skills in Microsoft Office word processing, presentation, and calculation software, eCRF, clinical trial management system, electronic trial master file
What we offer
Flexible working hours
Mobile Working up to 40%
At least 25 days of holidays
Friday after Ascension is a paid absence day
Training and further development opportunities
Company canteen with various options
Discounts for public transportation or affordable parking options
Teleflex 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
[email protected]
Diversity 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.
At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.
Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, QuikClot™, LMA™, Pilling™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.
