Unsere Kunden sind Unternehmen aus den Bereichen Pharma/ Biotech/ Medical Device mit Sitz in der Schweiz
- Pharma / Biotech / Medical Device
- Career progression
Unsere Kunden sind Unternehmen aus den Bereichen Pharma/ Biotech/ Medical Device mit Sitz in der Schweiz
- Grosses Netzwerk innerhalb der Schweizer aus der Life Science Industrie
- Vielfältiges Portfolio von in der Schweiz ansässigen Pharma-, Biotech- und Medic
For our client, a Pharmaceutical company in Zürich, we are urgently looking for an Health Economist Contractor to start at the 7th of June 2021 for a 6 months contract which can be extended.
- International Pharma Company in Zurich
- Start ASAP - 6 Months Contract
For our client, a Biopharmaceutical company based in Solothurn, we are looking for a Project Engineer CQV to start ASAP for a 12 months contract which can be extended.
- International Pharma Company in Solothurn
- Start ASAP - 12 Months Contract
Our clients are a diverse portfolio of company based in Switzerland
- Pharma / Biotech / Medical Devices Companies
- Career progression
Our clients are a diverse portfolio of company based in Switzerland
- Big network within the Swiss Life Science Industry
- Diverse portfolio of Swiss based Pharma, Biotech and Medical Device clients
If you have a Quality Assurance background and would like to be aware of all the open positions across Switzerland, join our talent Pool. We will make sure you are aware of the most interesting opportunities based on your seniority level and career expectation.
- Pharma & Biotech
- We work with all major players in the market
Operational and regulatory support for submission and maintenance activities, including preparation and submission of regulatory dossiers, maintenance of regulatory databases and archives.
- Temporary opportunity for the Pharmaceutical Industry
- Fast-growing and global organisation
Our client is a leading consumer dental-care company in Switzerland focusing health products as well as complementary dental and medical products.
- Exiting opportunity to join the Swiss Life Science Industry
- Have the chance to join a world leader in advanced technologies
- Ensure local GxP software compliance with regulatory requirements.
- Project for at least 1 year
- Responsible for ensuring local GxP compliance
- Quality Assurance Specialist (1 year contract)
- Main duties for the position is to focused around non-laboratory support of the QC functions.
- Data analysis, data trending, project and testing coordination, product and material specification management, inspection support, investigation leads, operational excellence leads, document revisions, initiating/completing quality systems, method/equipment validation and method projects activities.
- Responsible for operational, technical and compliance oversight
- Experience in OOS/OOT investigations
I am currently supporting a Swiss service provider company for pharma packaging who is currently looking for a QA System Manager.
- Swiss Pharma Company
- Career progression
I am currently supporting a Swiss service provider company for pharma packaging who is currently looking for a QA Engineer.
- Swiss Pharma Company
- Career progression
In this Role you will act as our clients FvP for the entities in Switzerland and perform the direct technical supervision, ensuring the correct handling of medicinal products and fulfilling the obligations. You sign for the quality of the medicinal products produced, in particular also taking into account the requirements of marketing authorization and EU GMP / GDP-Guideline.
- Global pharmaceutical company
- Leading the Quality team of 8 employees
We are looking for a Director QA GCP/GVP.
You will be responsible to ensure quality oversight and support the Clinical research and Drug Safety activities. In this role you will work with relevant stakeholders across our clients organization: R&D (Clinical Dev/Drug Safety, RA), Medical Affairs, Commercial, Technical Operations and Global Quality.
- international biopharmaceutical company
- exciting opportunity building new Quality Department in Switzerland
Our client is looking for a Senior Regulatory Affairs Specialist to join a small team in order to support the expansion of Regulatory Affairs activities (MDR, PMS, R&D) on innovative class III devices.
- Class III Medical Devices
- Innovative start-up
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
We are looking for candidates with a scientific background. Would you like to be aware of all the open positions across Switzerland? Join our talent Pool.
We will make sure you are aware of the most interesting opportunities based on your seniority level and career expectation.
- Pharmaceutical and Biotech companies in Switzerland
- We work with all major players in the market
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 der analytische Durchflusszytometer sowie Reagenzien in der klinischen FACS-Diagnostik und Forschung im Rahmen der gesetzten Ziele und Strategien für Ihr Vertriebsgebiet sowie die Realisierung der Umsatz- und GP-Ziele im zugewiesenen Verantwortungsbereich.
- ist eines der größten internationalen Medizintechnologie-Unternehmen
- eine berufliche Herausforderung in einem hochmotivierten Team
