20 annunci per il ruolo di regulatory affairs manager - switzerland (recruiting in corso)

Jr Regulatory Affairs Manager
Teleflex —Bülach, ZH
- Inglese
- Microsoft Office
- Competenze analitiche
Regulatory Affairs Manager (80%)
AbbVie —Cham, ZG
- Part-time
- Parzialmente remoto
- Inglese
- Master
- Bachelor
P2624 - Global Regulatory Affairs Specialist/Manager
Debiopharm —Losanna, VD
- 100%
- Parzialmente remoto
- Dottorato
- Inglese
- Master
Candidatura rapida
Scientific Communications Manager
Nobel Biocare —Kloten, ZH
- Gestionale
- Dottorato
- Capacità di scrittura
Medical Affairs Manager - Switzerland
OM Pharma Ltd. —Villars-sur-Glâne, FR
- Dottorato
- Inglese
- Master
Regulatory Affairs Director - Topical Pain
Haleon —Nyon, VD
- 100%
- Dottorato
- Master
- Bachelor
9 giorni
Medical review and affairs manager
Sobi —Zugo, ZG
- 100%
- Parzialmente remoto
- Inglese
- Bachelor
- Reti informatiche
Candidatura rapida
Manager, Professional Education
Edwards Lifesciences —Nyon, VD
- 100%
- Gestionale
- Inglese
- Master
Director, Policy, Advocacy and Government Affairs Switzerland
CSL Behring —Berna, BE
- 100%
- Inglese
- Competenze analitiche
Product Compliance Manager - Medical Devices (w/m/d)
Digitec Galaxus AG —Zurigo, ZH
- Part-time
- Remoto
- Microsoft Excel
- Servizio clienti
- Master
- Lavoro da casa
Senior Manager, CRM Medical Affairs, EU/NM
BeiGene —Basilea, BS
- CHF 148’600 - CHF 185’700 all'anno
- 100%
- Bachelor
- Leadership
- Capacità di comunicazione
Senior Manager, Market Access Specialty Care
Sobi —Basilea, BS
- 100%
- Remoto
- Dottorato
- Inglese
- Master
Candidatura rapida
Engagement Manager
NNIT A/S —Basilea, BS
- Gestionale
- Inglese
- Master
4 giorni
P2626 - Global Program Regulatory Lead
Debiopharm —Losanna, VD
- 100%
- Parzialmente remoto
- Gestionale
- Dottorato
- Inglese
Candidatura rapida
14 giorni
Corporate Legal Counsel (All Genders)
WIK Switzerland GmbH —Luzern, LU
- 100%
- Inglese
- Master
- Produzione
Candidatura rapida
Senior Manager R&D Quality Analytics & Portfolio Insights
BeiGene —Home Office
- CHF 74’500 - CHF 177’300 all'anno
- 100%
- Remoto
- Esperienza di laboratorio
- Ricerca
- Microsoft Office
Scientific Affairs Manager (all genders) 100%
Borer Chemie AG —Zuchwil, SO
- 100%
- Gestionale
- Inglese
- Project management
Product Manager
Symbios Orthopédie S.A. —Yverdon-les-Bains, VD
- 100%
- Gestionale
- Capacità di scrittura
- Inglese
Manager, Int’l Health Systems Integrations
Abbott Laboratories —Zugo, ZG
- Weekend
- Spagnolo
- Inglese
- Bachelor
Sr Clinical Research Mgr
MiniMed —Tolochenaz, VD
- 100%
- Gestionale
- Dottorato
- Ricerca

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Jr Regulatory Affairs Manager

Teleflex -
Bülach, ZH

Candidati adesso

Dettagli della posizione

Qualifiche

Inglese
Microsoft Office
Competenze analitiche
Bachelor
Adobe Acrobat

Descrizione completa della posizione

Date: Aug 22, 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 affairs manager offerte - switzerland

Jr Regulatory Affairs Manager

Regulatory Affairs Manager (80%)

P2624 - Global Regulatory Affairs Specialist/Manager

Scientific Communications Manager

Medical Affairs Manager - Switzerland

Regulatory Affairs Director - Topical Pain

Medical review and affairs manager

Manager, Professional Education

Director, Policy, Advocacy and Government Affairs Switzerland

Product Compliance Manager - Medical Devices (w/m/d)

Senior Manager, CRM Medical Affairs, EU/NM

Senior Manager, Market Access Specialty Care

Engagement Manager

P2626 - Global Program Regulatory Lead

Corporate Legal Counsel (All Genders)

Senior Manager R&D Quality Analytics & Portfolio Insights

Scientific Affairs Manager (all genders) 100%

Product Manager

Manager, Int’l Health Systems Integrations

Sr Clinical Research Mgr

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