- InternationalPermanentCHF161,309 - CHF230,441
For one of our top clients we are recruiting for a Senior Director, Qualified Person for Pharmacovigilance (QPPV). We are looking for a candidate who has a strong analytical mind and an eye for detail. Are you flexible, accurate and do you have good planning skills? Then we might be looking for you!
Innovative work environment
Excellent annual salary up to € 200000 gross
Save Job View Job - LausannePermanent
The Senior Director will be responsible for managing all aspects of operational plans across a program with multiple global clinical trials and serve as a leader to the clinical operations team and a key member of the clinical development department. The position will report to the Head of Global Clinical Operations based in the US.
Fast growing start-up organization
Leadership role
Save Job View Job - NyonPermanent
Prepare and coordinate various activities to make applications for product licenses.
Great opportunity to join a market leader in medical device.
International exposure.
Save Job View Job - LausanneTemporary
The Regulatory CMC Specialist is responsible for preparing and updating the CMC sections of assigned products (Rx and OTC drugs). Support the RA Managers for regulatory strategy of development and commercial products.
International company
Large product portfolio
Save Job View Job - GenevaTemporary
To handle life cycle management activities at an European level.
Prescription drugs
European scope
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Our client is looking for a Regulatory Affairs Manager to obtain registration for new specialty products in Europe and to ensure that the registrations for existing marketed products are maintained.
Small sized company
Prescription drugs
Save Job View Job - GenevaPermanent
This position will include acting as an clinical expert/liaison by engaging with targeted leads, providing education on the clinical utility of rapid molecular syndromic testing to current and future customers
Diagnostic solutions
To provide education to physicians
Save Job View Job - LausannePermanent
Manages Regulatory Affairs activities for all new and existing product development, including development of regulatory requirements/strategies.
Software products - Class IIb
Global role
Save Job View Job - BaselPermanent
Our client is currently looking for a passionate Regulatory Affairs professional to lead the European Cluster. This position requires strategical thinking as well as a hands on regulatory approach.
innovative medical device company
good global development options
Save Job View Job - SolothurnPermanent
Our client is looking for an experienced Quality Engineer to support the local production team in all quality assurance related questions. You will be responsible for all Quality Processes as well as the liaison of quality topics between several stakeholder.
innovative company with gloabl reach
very good development options
Save Job View Job - SolothurnPermanent
Our client is looking for an experienced Quality Manager to support the local production team in all quality assurance related questions. You will be responsible for the management of the on site Quality Expert as well as the liaison of quality topics between several stakeholders
innovative company with gloabl reach
very good development options
Save Job View Job - LausannePermanent
The Clinical will assume a leadership role in overseeing the design, implementation, conduct and evaluation of oncology clinical trials to ensure data quality and integrity.
Fast growing start-up organization
Innovative drug development
Save Job View Job - GenevaPermanent
Management of Phase II/ Phase III global clinical studies activities including a small team to manage.
Listed Biotechnology Company
Fast growing environment
Save Job View Job - SchwyzPermanent
The Global RA Manager is responsible to develop and implement the global RA strategy, as well as lead the RA business unit cluster.
Market leading consumer goods industry player
Senior role with Global reach
Save Job View Job - NyonPermanent
Our client is looking for a Technical Documentation Coordinator to support its regulatory affairs team.
Great opportunity to join a market leader in medical device
To be part of the regulatory affairs team
Save Job View Job - GenevaPermanent
Our client is looking for a Training and Education Manager to extend its team and development.
Work for a company which is a Pionner in its field
Promote and sell innovative products
Save Job View Job - LausanneTemporary
Global scope of activities.
Fast growing company.Global scope of activities
Fast growing company
Save Job View Job - ZugPermanent
You will be responsible to manage day to day regulatoty affairs challenges as well as additional projects related to global regulatory affairs strategy implementation.
This position gives you the opportunitiy to work with cutting edge technology as well as some of the best talents of the industry.innovative medium sized medical devices business
potential to develp personally and professionally
Save Job View Job - La Chaux-de-FondsPermanent
Afin de compléter son équipe Qualité et Affaires Réglementaires, notre client recherche un Responsable Affaires Réglementaires.
Autonomie
Large portefeuille de produits
Save Job View Job - ZugPermanent
The succesfull candidate will improve operations by bringing systematic and disciplined approach to risk management, control and governance processes. A thorough knowledge of ISO 13485 and FDA QSR are required.
Join a leading global medical devices player
Help people around the globe leading a healthier life
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