Zur weiteren Verstärkung Teams suchen wir im Bereich Marketing & Sales Delivery Systems am Standort Burgdorf eine engagierte Persönlichkeit
- leading developer and manufacturer of injection and infusion systems
- opportunity to shape an innovative and fast-phased medtech environment
Sie verantworten den erfolgreichen Verkauf von analytischen Durchflußzytometer sowie Reagenzien aus den Bereichen Pharmingen und Immunzytometrische Systeme) im Rahmen der gesetzten Ziele und Strategien für Ihr Vertriebsgebiet sowie die Realisierung der Umsatzziele im zugewiesenen Verantwortungsbereich
- Bei einem weltweit führenden Medizintechnikunternehmen
- Eine berufliche Herausforderung in einem hochmotivierten Team
Für unseren Kunden, einen internationalen key player im Bereich OTC, suchen wir per sofort oder nach Vereinbarung einen Account & Access Manager für die Zielgruppe Hospital/Spitäler in der deutschsprachigen Schweiz. Der Account und Access Manager ist ein fachlicher und kommerzieller Experte der die Spital-Strategie mit-entwickelt, anpasst und erfolgreich umsetzt.
- Internationales Pharmaunternehmen
- Sie haben Kundenbeziehungen im Bereich Hospital & Medical
- Quality Operations activities management with CMOs
- Elevate performance of contractors and identify, negotiate, implement and follow-up of process and systems improvements.
- ASAP - QA 6 months project
- Biotech company
Responsible for performing batch record review, procedures and standards at a TPM site to ensure compliance with regulatory and corporate requirements.
- Quality Compliance Specialist
- Temp 12 months - Start ASAP
Supervises the activities of manufacturing, supply chain of medical devices. Involved in directing a team in charge of manufacturing, design transfer to manufacturing, manufacturing process validation, supply chain management. Responsible for proper supplier management per our Quality Management System. Oversees production forecast.
- Medical device - Class 3 - ISO13485 - startup
- Manufacturing, design transfer, process validation, supply chain management
Montage et assemblage de précision de pièces sur une plateforme de diagnostic.
- Start-up innovante - dynamique - Medical device - IVD
- Assemblage de précision - Vérification - Empaquettage
Préparer et coordonner les enregistrements des produits (Dispositifs médicaux Class I, IIa) sur les marchés hors Europe.
Effectuer et maintenir à jour les listings des dispositifs médicaux en Europe et aux USA.
- Enregistrements internationaux
- Entreprise à taille humaine
Participez et suivez la réalisation technique des nouveaux produits et le support des produits existants en production et apportez votre contribution à l'amélioration continue. Poste basé près de Fribourg.
- Leader international dans les équipements de diagnostics
- Support production - Transfert technique - Test de validation
En tant que Responsable Amélioration Continue h/f, vous serez en charge du déploiements des outils Lean/6-sigma sur l'ensemble du site, et de la définition des projets liés. Poste basé sur Yverdon-les-Bains.
- Entreprise internationale - Equipements médicaux - Innovante
- Lean Manufacturing - Excellence Opérationnelle - 6-sigma - DMAIC
As Senior HW System Engineer m/f, you will be responsible to understand the assay workflow requirements for integration
onto the instrument; interpret the assay needs and develop associated design inputs, with specific focus on hardware and software development requirements. Subsequently supporting instrument development, assay integration and verification/validation activities. Position based next to Lausanne.
- International company - In-Vitro Diagnostic - Medical device (Class III)
- instrument development - Assay integration - Project Management - ISO13485
I am currently supporting a medium Medical Device company who is currently creating a new position as Qualification/Validation Engineer as they are in constant growth.
- Growing Medical Device
- Career progression
As BioEngineer m/f, you will have a leading role in the development of assay technologies the company platform. Position based in Lausanne.
- BioTech - Innovation - Fast-growing company
- Assay technology development - Experiments and analysis of data
As Director Hardware Engineering m/f, you will be the process owner for the Mechanical/Electrical/Automation engineering, and embedded SW/HW. And you will also ensure the compliance with all applicable standards and procedures. Position based in Lausanne area.
- International start-up - Innovative - Medical device (Class III)
- Team management - Quality compliance (Mechanical/Embedded electronics)
Manage immunoassay development and improvements projects as well as resources to meet deliverables and deadlines
Resource management and coaching of team members (e.g. Lab Technicians and Interns).
- Fast growing company - Diagnostic - IVD
- Immunoassay development and improvements projects
The QA Manager, GVP is responsible for:
Ensuring quality oversight and support of the PV activities
Build and develop the audit strategy, program and plans within the PV area
Perform and coordinate PV audits internally, Partners and externally at external service providers
Support and collaborate with Drug Safety,Medical Affairs, Regulatory Affairs and Affiliates as necessary
- international biopharmaceutical company
- exciting opportunity building new Quality Department in Switzerland
For our client, an international Pharmaceutical Company in the greater Zurich area, we are urgently looking for an Junior and Senior Quality Assurance Specialist Pharma to start ASAP for a 12 months contract which can be extended.
- International Pharma Company in Zurich
As QC and Analytical Development Laboratory Manager (m/f), you will be responsible for managing the QC/analytical laboratory in accordance with cGMP and company requirements, and also be responsible to resolve problems with instruments, test methods, lab chemicals, standards, and samples.
- Medical device - Class III - International group
- Laboratory - Quality Control - Team Management
As an Automation Engineer m/f, and part of the team, your main tasks will be :
- Coordinate and execute daily activities and troubleshooting in the HMI/PLC of stand alone systems.
- Execute projects improvements and modifications in the HMI/PLC of stand alone systems.Work closely with the vendors and installation contractors
- Report to the Responsible Engineer Automation.
- International company - Bioengineering
- Automation - Programming - HMI/PLC systems - Troubleshooting
The Manager CMC Project will manage CMC product development for several Biosimilar products going into and through clinical development stages.
- Expanding biotech company
- Biologics
