- GenevaPermanentCHF80,000 - CHF85,000
Renforcement de la marque de notre client sur la Suisse romande, ouverture de points de vente et augmentation des assortiments. Formation et animation des points de vente (pharmacies).
Marque attractive et innovante
Environnement dynamique
- La Chaux-de-FondsPermanent
Gestion du processus d'évaluation clinique des dispositifs médicaux développés et commercialisés par l'entreprise, afin de garantir la conformité aux exigences générales de sécurité et de performance requises dans les réglementations en vigueur et à venir (MDR et autres).
Environnement évolutif
Nouvelle fonction multitâches
- ZürichPermanent
Als Projektleiter im Qualitätsmanagement übernehmen Sie die Verantwortung für spezifische Projekte und stellen die Konformität des bestehenden Qualitätsmanagementsystems nach ISO13485 sicher.
Dynamisches Schweizer Industrieunternehmen
Vielfältiges Aufgabengebiet
- ZugPermanent
The world leader of blood glucose monitoring systems is currently seeking a Health Care Compliance Manager to strengthen its global team.
Join the Leader of blood glucose monitoring systems in a role with global reach
Be a key member of the health care compliance team
- St. GallenPermanent
Der „Medical Affairs Specialist" bildet die Schnittstelle zwischen internen Abteilungen und ist der wichtigste Ansprechpartner bei medizinischen Fragen. Die mehrfach patentierte und im Markt führende Technologie unseres Kunden wird über Direktfachvertrieb und entsprechende Landesvertretungen in mehreren Ländern vertrieben.
Ausarbeitung und Durchführung von klinischen Studien
Mitarbeit bei Beantwortung von medizinischen Anfragen
- GenevaPermanent
Build and implement CMC project plan based on the global strategy.Fast growing environment
Great opportunity to join a fast growing biotech company
- ZugTemporary
As a talented developer and co-ordinator of innovative and highly rated external medical education programs, you will be responsible for ensuring the delivery of best in class medical and scientific education via channels having an international reach, and for collating, reporting on, and responding to unmet medical educational needs.
Immediate availability required
Truly international organization
- SolothurnTemporary
As Senior Indirect Buyer you build up relationships with Key stakeholders, identifying and leading cross-functional teams, developing and managing the sourcing implementation plans, and performing all business related functions of the sourcing initiative, negotiating contracts, and transitioning to the business units for physical implementation.
Immediate availability required
Dynamic international organization
- LucerneTemporary
The EMEA Compliance Manager is part of the Regional Transformation team working directly with the SCM Quality team. The function oversees and supports documentation management, training management, L&D support, compliance/transformation projects deviation & related SOP reviews/approvals. The respective compliance/transformation projects are to drive Supply Chain optimization towards the Global Quality Manual Standards & the EMEA hubs to be Permanently Inspection Ready.
Global pharmaceutical organization
Immediate availability required
- LucerneTemporary
An exciting opportunity for a Specialist Engineering with main focus to Computer System Validation (CSV) and Data Integrity (DI) to join the biological drug development and manufacturing site
Immediate availability required
Contrat of unlimited duration
- LucerneTemporary
Provide ongoing support for a Quality Assurance team such as review of documents for final disposition of clinical supplies to clinics.
Review of documents for final disposition of clinical supplies to clinics, including label release, GMP batch record review for packaging activities, regulatory review for compliance against filings
Global pharmaceutical organization
Immediate availability required
- LucerneTemporary
The Associate Director Clinical Project Manager will be responsible for the oversight in compliance related matters, for conducting the cross functional Study Execution Team, and for continuous monitoring of KPIs and Metrics compliance of vendors for assigned complex clinical trials. Moreover you manage the study budget, including Task Orders, Change Orders, invoice approval and financial reconciliation process
Challeging opportunity within a global pharmaceutical organization
Interim 12- months assignment
- BaselPermanent
For one of our key clients in Switzerland, we are currently recruiting a QA/QC manager.
This role has been opened to strengthen the current team.
Join the Leader in the industry
Become a key member of the QA team
- 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
- LausannePermanent
We are looking for an Intellectual Property Associate.
Growing Biotech Company
Intellectual Property - One Year contract
- MorgesPermanent
Oversee and support the requirements related to the EMEIA tender process, support the global regulatory intelligence and regulatory surveillance processes, advocacy with government bodies and manufacturer associations across Europe, implementation of new regulation, tender management.
Innovative Medical Company
Dynamic environment
- NyonPermanent
Prepare and coordinate various activities to make applications for product licenses.
Great opportunity to join a market leader in medical device.
To be part of the regulatory affairs team.
- 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 support the regulatory affairs team
- ZugPermanent
Become a Key member of the RA team helping clearing advertising and promotional material.
Join a leading global medical devices player
Be a key member of the Regulatory Affairs team
- GenevaTemporary
S/he has the responsibility to support dossier preparation for new medicine registration application.
Great opportunity to work on a new medicine registration application
Rare diseases
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