- LausannePermanent
Our client is seeking an IP Group Leader, who is responsible for managing the Intellectual Property portfolio and leading the IP group of IP associates.
Fast growing company
Innovative therapies
Save Job View job - SolothurnTemporary
Für unseren Kunden, ein Pharmaunternehmen in der Nähe von Basel, suchen wir einen «Senior Maintenance Manager» für ein 12-monatiges Projekt mit der Option zu Verlängerung.
Stark wachsendes und dynamisches Pharmaunternehmen in Solothurn
Min. 12 M Vertrag mit Potential auf mehr - Teil eines motivierten Teams
Save Job View job - SolothurnTemporary
For our client, a Medical Health Care company, we are looking for a Process Expert to start at the 7 th of December 2020 for a 12 months contract which can be extended.
Experience in developing quality processes
Fast-growing company
Save Job View job - ZugTemporary
Our clients are a diverse portfolio of companies based in Switzerland.
Looking for new opportunities in a Life Science Company?
3+ Years Experience in Quality Assurance in Pharma or Medical Device?
Save Job View job - ZürichPermanent
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
Save Job View job - InternationalTemporary
The QA Associate is responsible for supporting the RA/QA department in the execution, maintenance and improvement of existing quality processes, and take part in the deployment of VEEVA.
Biotech company
Quality Management System (QMS) - SOP officer - System implementation
Save Job View job - ZugTemporary
The QA Operations Associate III assures that all operations meet or exceed cGMP regulations ensuring the quality Bulk Drug Substance, cell bank supporting on shop floor the daily manufacturing, Warehouse and facility operations.
Experience with facility construction and start-up is an asset
Welcoming atmosphere and good team spirit
Save Job View job - ZugTemporary
For our client, a Medical Health Care company, we are looking for a Pharmacovigilance Manager to start at the 2nd of November 2020 for a six months contract which can be extended.
Globally active Swiss Pharmaceutical Company
Knowledge of Good PHARMACOVIGILANCE Practices
Save Job View job - LausannePermanent
The Senior IP Associate, Biology will be responsible for managing the patent portfolio related to biologics and technology platforms.
Innovative company
Start-up
Save Job View job - InternationalPermanent
Operative und disziplinarische Führung von ca. 200 Mitarbeitern. Sie verantworten als Standort-Geschäftsführer die Geschäftsergebnisse und steuern den gesamten Fertigungsprozess mit besonderem Schwerpunkt auf die Einhaltung der vereinbarten Qualitäts-, Produktionsleistungs- und Lieferziele, sowie der Sicherheitsstandards.
Geschäftsführer / Werksleiter
Pharmaindustrie
Save Job View job - InternationalPermanent
Personalführung und Weiterentwicklung des Laborteams
Entwicklungslabor
Gestaltungsspielraum
Save Job View job - LausannePermanent
The position will act as the European regulatory lead on certain development programs, providing regulatory guidance and oversight. The position will be responsible for management of all EU regulatory activities in this regard including management of regulatory service providers.
Expanding biotech company
Oncology
Save Job View job - ZugPermanent
The Sr. RA Manager will be supporting the European and US American BU heads in all Regulatory topics as well as take on communication with the relevant authorities.
Exciting new Product Launch Project
Flexible work environment
Save Job View job - SolothurnPermanent
Are client provides a complete range of technologies and services for reliable injection systems for self medication making them one of the market injectable leaders. With over 35 years of experience they are looking for a experience Regulatory Affairs Manager to join there international team
Exiting opportunity to join the Swiss Life Science Industry
Diverse Swiss based medical technology company
Save Job View job - GenevaPermanent
The Associate Director of Medical Affairs Surgical' primary responsibility is to develop and execute a comprehensive medical affairs plan that contributes to the achievement of achieves our client's short- and long-term goals.
Surgical Medical Devices
Fast growing activity
Save Job View job - SwitzerlandPermanent
You are interested in a new challenge within the Medical Affairs department or as MSL, in one of Switzerland's most reputable Life Science companies. Apply below and one of our consultants will contact you for a first assessment.
big network within the Swiss Life Science Inudstry
diverse portfolio of Swiss based Pharma and Medical Device clients
Save Job View job - ZugPermanent
The RA Manager is mainly responsible for leading all activities related to the current MDR change project. Additionally this role will be in charge of global submissions and other regulatory tasks.
Internationally renowned Life Science company
Good opportunities for professional development
Save Job View job - BernPermanent
The R&D Project Manager is responsible for the continuous improvement and expansion of our clients product portfolio.
Working with globally leading products
Flexible work environment
Save Job View job - ZürichPermanent
- The exiting opportunity to join a global leader with over 60 years of experience in the market
- To be part of a multicultural environment based in Switzerland but operating in over 100 countries
- We are looking for a strong and hands on regulatory manager to join the team that offers diagnosis equipment and therapeutic support, in the areas of cardiac rhythm management
Exiting opportunity to join the Swiss Life Science Industry
Diverse Swiss based medical technology company
Save Job View job - SwitzerlandTemporary
On behalf of our Client we are looking for an experienced Medical Writer to create scientific and regulatory documents in accordance with EU On behalf of our Client we are looking for an experienced Medical Writer to create scientific and regulatory documents in accordance with EU In Vitro Diagnostic Regulation (IVDR) requirements.
The Client offers 2 years temporary contract and the possibility to work remotely.In-Vitro Diagnostic
Dynamic local team in a multinational structure
Save Job View job
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