Natur- oder rechtswissenschaftliche Ausbildung im Kosmetik- / NEM-Umfeld Mind. 5 Jahre Berufserfahrung im Bereich Regulatory in einem produzierenden Betrieb in der Kosmetik- oder …
Mitglied der Geschäftsleitung Über Mepha und Teva in der Schweiz Mepha Pharma AG und Teva Pharma AG gehören zusammen zu den führenden Pharmaunternehmen in der Schweiz. Mepha is…
Company Description Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare dis…
Company Description Deciphera is a biopharmaceutical company focused on discovering, developing and commercializing important new medicines to improve the lives of people with ca…
Start date: As soon as possible Company Overview: is a fast-growing medical device software company headquartered in Bern, Switzerland. Our mission is to enable the right decis…
About the role As a Public Affairs Manager, you will be responsible for positioning Swiss Re as a thought leader and leading risk knowledge company. You'll be building Swiss Re's…
The United Nations (UN) Office for the Coordination of Humanitarian Affairs (OCHA) is the part of the United Nations Secretariat responsible for bringing together humanitarian acto…
By continuing to use and navigate this website, you are agreeing to the use of cookies. Accept Close Press Tab to Move to Skip to Content Link Search by Keyword Search by Lo…
Are you ready to shape regulatory strategies for Switzerland? Are you an ambitious and experienced regulatory affairs manager being ready to take the next step and thereby making a…
Our client is a major pharma player in Basel with a distinctive and unmistakable image, carrying very strong brands. The purpose of the Contract & Process Manager is to support the…
Company Description medmix is a global leader in high-precision delivery devices. We occupy leading positions in the healthcare, consumer, and industrial end-markets. Our custome…
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed…
At neustark, we’re all in for one mission: permanently removing one million tons of CO2 in 2030, and even more every year beyond that. Why? It’s a no-brainer: we want to enable a b…
Provide Regulatory strategies for projects as RA representative in cross-functional teams Responsible for regulatory Assessment on product changes Coordinate the preparation of r…
Support team members in creating CE Mark submissions and change notifications to our Notified Body (NB), including responding to regulatory inquiries Aid in the completion and upk…
Directs the preparation and coordination of comprehensive regulatory submissions for Medical Devices, ensuring compliance with local and international regulations and achieving com…
Your main Accountabilities You enjoy the regulatory and sustainability world and are always up to date with its growing complexity and its related business implications. You unde…
Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, …
Job Purpose Be a member of product development project-teams from the initiation phase, ensure implementation of quality and Regulatory Affairs requirements for Europe, US & Cana…