20 meilleures offres (regulatory specialist, zürich zh) (à pourvoir)

Asc Regulatory Affairs Specialist (3-year contract)
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Cryptonow —Zoug, ZG
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- 100%
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Julius Baer —Zürich, ZH
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JayBee AG —Zoug, ZG
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Consultant – Risk, Controls and Internal Audit
KPMG —Zürich, ZH
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Julius Baer —Zürich, ZH
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Asc Regulatory Affairs Specialist (3-year contract)

Teleflex -
Bülach, ZH

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Détails de l'emploi

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Logement

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Anglais
Microsoft Office
Esprit d'analyse
Niveau Licence
Adobe Acrobat

Description complète du poste

Date: Jul 24, 2026

Location: Bülach, ZH, CH

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Company: Teleflex

Expected Travel: None

Requisition ID: 14000

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

In regulatory we are responsible for ensuring that vascular intervention medical devices are developed, manufactured, and distributed in strict compliance with global healthcare laws registrations and for submission and approval in highly regulated countries including Europe, US and Canada.

Principal Responsibilities
Assessment of design and manufacturing changes to ensure compliance with regulatory requirements and that sufficient information is available to perform the regulatory impact assessment of the change
Coordinate and contribute to worldwide assessment of changes and support the related product and production lifecycle activities
Maintain regulatory documentation up to date for worldwide regulatory purposes
Support the registration of changes for class II and III devices in the CE, US, Japan and other highly regulated countries
Coordinate and submit deficiency responses to relevant certification bodies and country authorities
Education / Experience Requirements
University degree in natural science, pharmacy, pharmacology, medicine or engineering
At least 2 years of experience with the registration of medical devices and regulatory assessment of changes in Europe and other highly regulated countries
Literate in Microsoft Office and Adobe Acrobat applications
Reliable and communicative personality
Ability to work in multidisciplinary teams with different backgrounds (R&D, Production, Quality, Marketing, Clinical)
Attention to details, excellent organization and analytical skills, and ability to work simultaneously on multiple and sometimes urgent projects with tight timelines.
Ability to adapt to program/timeline changes as needed
Fluency in English is mandatory
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.

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regulatory specialist emplois - zürich zh

Asc Regulatory Affairs Specialist (3-year contract)

Regulatory and Start Up Specialist - Switzerland

Regulatory Affairs Specialist (60%)

Avaloq Developer - Parametrization Specialist Regulatory Reporting 100%

Junior Compliance Specialist - Conduct Framework Employee Compliance 100% (f/m/d)

Clinical Specialist - Interventional, Austria & Switzerland

EHS Specialist

Site Start-Up Specialist based in Switzerland

Medical Science Liaison Manager (MSL) and Medical Advisor - Switzerland

Sponsor Dedicated Site Budget & Contract Specialist based in Switzerland

Legal Counsel / Contracts Specialist for ETH Zurich | Space

Customer Care Specialist (CH & EU), Zug (CH)

Laboratory Specialist Performance Verification (m/f/d)

Junior Compliance Officer – Market Abuse Monitoring Specialist 40–60% (f/m/d)

Senior Specialist - Employee related Conflicts 80-100% (f/m/d)

Multi-Asset Execution Specialist, Zürich, 100% (f/m/d)

R&D and TS&D Laboratory specialist (f/m/d)

Compliance Specialist Crypto, 80-100%, Zug & remote

Consultant – Risk, Controls and Internal Audit

Operations Specialist for Derivatives Processing 100% (f/m/d)

Je souhaite recevoir la dernière alerte Emploi pour les postes de ce type : regulatory specialist (zürich zh)

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