Regulatory affairs specialists Lavori in Switzerland
Ultimo aggiornamento: 11 ore fa
Would you like to join and contribute to a successful and growing multi-national organization in the heart of Europe and one of the world’s leading regions of the pharmaceutical industry? Veristat ...Mostra di piùUltimo aggiornamento: 7 giorni fa
At Distalmotion, we believe that every patient undergoing minimal invasive surgery should benefit from the best of surgical expertise and robotic technology.
This is the vision that made us create D...Mostra di piùUltimo aggiornamento: più di 30 giorni fa
Regulatory & Clinical Affairs Specialist.Experts in developing devices for minimally invasive surgery and imaging, my client in their growth phase has partnered with me to find the right fit! We ar...Mostra di piùUltimo aggiornamento: 29 giorni fa
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Regulatory Affairs Manager
Randstad SwitzerlandZürich, Zürich, Switzerland For our client, an international pharmaceutical company, we are looking for a.As a Regulatory Affairs Manager, you will define, develop, and lead Global Emerging Markets (GEM) strategies to maximiz...Mostra di piùUltimo aggiornamento: 11 ore fa
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Manager, Regulatory Affairs
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Regulatory Affairs
Kodiak SciencesSwitzerland Kodiak Sciences aspires to global leadership in ophthalmology by aggregating top talent, technologies, discoveries, and ideas.
We are working to develop disruptive products and platforms to prevent ...Mostra di piùUltimo aggiornamento: più di 30 giorni fa
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These regions are also often deprived of innovative therapies developed in t...Mostra di piùUltimo aggiornamento: 1 giorno fa
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VeristatBaselTempo pieno
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Regulatory Affairs Manager
K-Recruiting Life SciencesZürich, Zürich, Switzerland Regulatory Affairs Manager (M / F / D).Defines, develops and leads GEM strategies to maximize regulatory success towards achievement of program objectives.
Independently manages, plans and executes all ...Mostra di piùUltimo aggiornamento: 11 ore fa
Regulatory Affairs Specialist
Distalmotion SAÉpalinges, VD, CHQuick Apply
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Regulatory & Clinical Affairs Specialist
headcount AGBern,Switzerland100.000,00 CHF–110.000,00 CHF annuale
Tempo pieno
Quick Apply
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Regulatory Affairs Manager
TN SwitzerlandSempach, Luzern, Switzerland The Global Regulatory Affairs department of the B.Braun Avitum division has an opportunity for a Regulatory Affairs Manager located at our site in Sempach, Switzerland.
In our plant in Sempach, we d...Mostra di piùUltimo aggiornamento: 11 ore fa
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Regulatory Affairs Specialist
TRB CHEMEDICA INTERNATIONAL SACarouge GE, CH TRB Chemedica is a major international pharmaceutical company, headquartered in Switzerland, specializing in the manufacturing and distribution of innovative therapeutic solutions in ophthalmology,...Mostra di piùUltimo aggiornamento: 12 giorni fa
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Regulatory Affairs Manager
Randstad (Schweiz) AGZürich, Zürich, Switzerland For our client, an international pharmaceutical company, we are looking for a Regulatory Affairs Manager, Market Products Development, Growth and Emerging Markets (GEM).
Department : Global Regulator...Mostra di piùUltimo aggiornamento: 11 ore fa
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Regulatory Affairs Manager
Proclinical StaffingZürich, Zürich, Switzerland Get AI-powered advice on this job and more exclusive features.Direct message the job poster from Proclinical Staffing.Senior Research Associate @ Proclinical Staffing - DACH | Engineering.Proclinic...Mostra di piùUltimo aggiornamento: 11 ore fa
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Regulatory Affairs Manager
Experis SwitzerlandZürich, Zürich, Switzerland Experis is the global leader in professional resourcing and project-based workforce solutions.On behalf of our Pharmaceutical company in Zurich, we are looking for a Manager Regulatory Affairs with...Mostra di piùUltimo aggiornamento: 11 ore fa
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FKG Dentaire SàrlLa Chaux-de-Fonds, CH Participate in the development and deployment of our regulatory affairs processes and report on their effectiveness and any need for improvement.
Manage the international registration of medical dev...Mostra di piùUltimo aggiornamento: 7 giorni fa
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Regulatory Affairs Manager
Proclinical GroupZürich, Zürich, Switzerland Proclinical is seeking a Regulatory Affairs Manager to lead the team, focusing on Marketed Products Development in Growth and Emerging Markets.
This role involves developing strategies to ensure reg...Mostra di piùUltimo aggiornamento: 11 ore fa
Regulatory Affairs Manager.
YpsomedSolothurn, Switzerland Focus of this position is supporting our rapidly developing Diabetes Care (active and connected devices).Manage the development and implementation of regulatory strategies.Support and prepare produ...Mostra di piùUltimo aggiornamento: più di 30 giorni fa
Regulatory Affairs Manager
ProclinicalZürich, Schweiz Proclinical is seeking a Regulatory Affairs Manager to lead the team, focusing on Marketed Products Development in Growth and Emerging Markets.
This role involves developing strategies to ensure reg...Mostra di piùUltimo aggiornamento: 4 giorni fa
REGULATORY AFFAIRS SPECIALIST
ERServicesLugano CH Laureain materie scientifiche (es.CTF, Farmacia, Biotecnologie etc);.Esperienzaminima di 2 / 3 anni maturata nel ruolo di Regulatory Affairs Specialist inambito farmaceutico;.Comprovataesperienza di ...Mostra di piùUltimo aggiornamento: più di 30 giorni fa
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Regulatory Affairs Manager
Randstad SwitzerlandZürich, Zürich, Switzerland11 ore fa
Descrizione dell’offerta di lavoroDefine, develop, and lead Marketed Products GEM (Global Emerging Markets) strategies to achieve program objectives and maximize regulatory success. Manage, plan, and execute all regulatory activities, including investigational applications, marketing applications, variations, post-approval reporting, and life-cycle management for assigned programs. Communicate regulatory strategies, submission plans, timelines, and impact assessments of regulatory trends and changes to key stakeholders. Stay current on regulations and guidelines in Growth and Emerging Markets (GEM) to assess their impact on drug development, registration, and life-cycle management. Provide regulatory expertise on marketed products in GEM, focusing on non-clinical and clinical aspects of registration and post-marketing compliance. Ensure fulfillment of international product approval conditions for late-stage programs and maintain compliance with registration requirements. Build strong relationships with Local Regulatory Leads, Regional and Global Regulatory Teams, cross-functional teams, and external consultants. Lead or support preparation for Health Authority (HA) meetings, represent the company as required, and ensure effective follow-up on outcomes. Collaborate with regional market access and local regulatory colleagues to align market access and reimbursement strategies with regulatory plans. Bachelor’s degree in a scientific discipline; advanced degree preferred Considerable experience in the pharmaceutical industry, including 4+ years of direct regulatory affairs experience in development and / or post-marketing phases. Solid regulatory experience, with knowledge of regulations and guidances for drugs and biologics in development and life-cycle management for growth and emerging markets, US, and EU; including interaction with Health Authorities. Preferred experience managing major regulatory filings and contributing to regulatory and / or development strategies. Ability to interpret complex scientific issues across multiple projects related to regulatory requirements and strategy. Strong communication, timeline management, and negotiation skills, with experience in regulatory strategy and risk mitigation. Proven ability to work independently and collaborate effectively within global teams and with senior leadership. Effective manager with experience bringing cross-functional teams together to achieve common objectives. Willingness to travel to various meetings, including overnight trips. Mid-Senior level Contract Other Industries : Pharmaceutical Manufacturing
For our client, an international pharmaceutical company, we are looking for a Regulatory Affairs Manager.
General Information :
- End date : 15.08.2025
- Department : Global Regulatory Affairs
- Remote / Home office : possible
About the job :
As a Regulatory Affairs Manager, you will define, develop, and lead Global Emerging Markets (GEM) strategies to maximize regulatory success, strengthen the product development plan, enable patient access, and achieve appropriate pricing and reimbursement in alignment with program objectives. This includes managing all aspects of submission processes and ensuring timely approval of investigational applications, marketing applications, and life-cycle management activities.
Tasks & Responsibilities :
Must-haves :
If this sounds like the perfect opportunity for you, we’d love to hear from you!
Submit your CV today and be part of a leading pharmaceutical company driving healthcare innovation.
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