- 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
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
Verantwortlich für die Entwicklung und Umsetzung der nationalen Market Access Strategie, sowie die Leitung des MA Teams.
Innovatives internationales Pharmaunternehmen
Fachexpertenposition mit Führungsverantwortung
Save Job View Job - ZugPermanent
- Aufarbeitung von klinischen Daten für die Abteilungen Sales & Marketing, wie auch alle Stakeholder die die Firma auf Fachveranstaltungen vertreten.
- Durchführung wie auch Entwicklung des bestehenden Weiterbildungsprogrammssehr innovatives Unternehmen
Position mit viel Potential für interne Entwicklung
Save Job View Job - LucerneTemporary
Manage the contractual relationship with vendors in capital investment projects.
Immediate availability required
Global pharmaceutical organization
Save Job View Job - SolothurnTemporary
Responsible for proving site based support during the Commissioning, Qualification and Validation phase, (CQV), of the DeltaV DCS system for the new Manufacturing facility. The primarly focus is on on the commissioning and qualification of the DeltaV DCS system in an assigned area(s); support of other integrated Operations Management Systems (DCS, PLC, MES and Manufacturing Data systems) may also be required.
Global dynamic organization
Immediate availability required
Save Job View Job - ZürichPermanent
The life of a recruitment consultant is fast paced, and requires many different skills. One day you could be pitching to a client, the next you may be interviewing candidates for a job. You will learn business development, professional customer service, revenue generation and much more. It's also a job where you change lives daily, for commercial clients and individuals.
Join the market leader in the recruiting industry
Supportive team environment and fostering ongoing learning and development
Save Job View Job - SolothurnTemporary
Responsible for supporting the quality management system on review and approval of validation and engineering documents, test protocols, CAPAs, deviations, change controls and any technical documentation where QA needs to approve before implementation and upon completion.
Immediate availability required
Global pharmaceutical organization
Save Job View Job - GenevaPermanent
Build and implement CMC project plan based on the global strategy.Fast growing environment
Great opportunity to join a fast growing biotech company
Save Job View Job - ZürichTemporary
In this challenging position you will support the CPLs for the planning, implementation, execution and compliance of operational plans for clinical study/program with multiple clinical vendors in order to maintain inspection readiness.
Short notice availability
Work in Zurich City
Save Job View Job - 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
Save Job View Job - 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
Save Job View Job - 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
Save Job View Job - GenevaPermanent
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
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