Regulatory Affairs Manager

We have an exclusive mandate for one of our clients in Medical Devices based in Canton of Neuchatel. As a Regulatory Affairs Manager, you will be responsible for: - Support new product development by using in-depth knowledge and understanding of US domestic and international medical device, regulations (including 510k, and International dossiers) - Lead...

Title: Manager, Regulatory Affairs (CMC)Hybrid working pattern: 2 WFHLocation: Basel or VispRelocation support is provided – subject to criteria.Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working...

**Regulatory Affairs Manager, Novartis, Basel, Switzerland** 1 unique opportunity to join Regulatory Affairs Team! Person on this position will take care of all drug regulatory affairs matters regarding the assigned indication group. Acts as an interface between global Regulatory Affairs departments and Swiss medic in order to obtain new marketing...

**DSM - Bright Science. Brighter Living.** **What you’ll do**: - As a Regulatory Affairs Manager, you will manage the regulatory compliance, market clearance, advocacy and business support of DSM animal nutrition products and provide advice to Marketing and Sales, Product Management, Global Regulatory in all regulatory related topics/issues for Animal...

Proclinical are recruiting a Regulatory Affairs Manager - CMC for a pharmaceutical organisation. This role is on a contract basis and is located in Basel. *** **Responsibilities**: - Offer regulatory assistance for projects and project teams. - Write, evaluate and offer contribution from a CMC perspective on pertinent documents necessary for clinical...

**Manager, Regulatory Affairs, International** One of Sobi’s four strategic pillars is to “Go Global”. The Manager, Regulatory Affairs International supports our ambitious geographical expansion plans. Sobi is seeking to register some of our existing portfolio into new territories and to register several of our development projects into the...

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description...

**The Life Science Career Network** Our client is a leading global player in the Pharmaceutical industry with global headquarters in Basel, Switzerland. They are undergoing a transformation with respect to culture and outside perception. The organisation focusses on novel therapies in Oncology and Ophthalmology and is also currently developing a...

Innovative Medikamente für Mensch und Tier: Dafür steht das forschungsbasierte Pharmaunternehmen Boehringer Ingelheim seit über 130 Jahren. Boehringer Ingelheim zählt zu den 20 führenden Unternehmen der Branche und ist auch heute noch ein Familienunternehmen. Jeden Tag schaffen rund 52.000 Mitarbeiter Werte durch Innovation in den drei...

**Regulatory Affairs Coordinator 4881 SRS** As the Regulatory Affairs Coordinator you will support the Regulatory team in managing, tracking and archiving regulatory requests received from our partners companies in their respective territories. **Main Responsibilities**: - Ensuring all documents/declarations/statements are signed by company...

Sie möchten Ihre Expertise gezielt in einer neuen beruflichen Herausforderung unter Beweis stellen, um Ihr Potential voll ausschöpfen zu können? Dann gehen Sie jetzt mit uns Ihren nächsten Karriereschritt! bruederlinpartner bringt als spezialisierter Personaldienstleister jeden Tag Fach - und Führungskräfte mit nationalen und internationalen...

**Quality Assurance & Regulatory Affairs (QA/RA) Manager - Medical Devices** ALTOGEN is a Swiss engineering and consulting company specialized in life sciences with proven expertise in pharmaceuticals, biotechnology, medical devices. With several years of experience, technical expertise and project coordination, we support our partners throughout all areas...

Innovative Medikamente für Mensch und Tier: Dafür steht das forschungsbasierte Pharmaunternehmen Boehringer Ingelheim seit über 130 Jahren. Boehringer Ingelheim zählt zu den 20 führenden Unternehmen der Branche und ist auch heute noch ein Familienunternehmen. Jeden Tag schaffen rund 52.000 Mitarbeiter Werte durch Innovation in den drei...

Unsere Mandantin ist ein Schweizer KMU, das sich in einer Nische im Pharmabereich erfolgreich etabliert hat. In ihrem Auftrag suchen wir eine Persönlichkeit mit ausgeprägtem Verantwortungsbewusstsein als Regulatory Affairs Manager Pharma EU/CH (m/w/d). **Arbeitsort**: Grossraum Zürich Aufgaben - Selbständiges Erstellen von...

**EINFÜHRUNG**: Our profession and our passion are "HR Management". Global Personal is an independent company of the Interiman Group SA with over 100 employees offering a complete range of services in the field of Human Resources at 21 locations in German-speaking Switzerland. For our client, an international technology company in Basel, we are looking...

REGULATORY AFFAIRS Associate Director, Europe (with focus on Switzerland) Regulatory Affairs, Basel, Switzerland Reports To: Director, Team Lead of EU Regulatory Affairs **Job Description**: The (Swiss) Regulatory Affairs lead will report to the team lead of Regulatory Affairs Europe and will have dotted line reporting to the Swiss General Manager. The...

Location: role can be located anywhere in Europe At Corza Medical, our mission is to support surgical providers with remarkable service, trusted performance, and outstanding value by creating an unmatched experience that stems from listening to the surgical experts themselves. Our product family is the result of years of experience championing surgeons and...

 Für das Unternehmen unseres Kunden in Basel suchen wir einen Drug Regulatory Affairs Manager 80-100% Tasks: Selbständige Erstellung und Pflege von Zulassungs- und Registrierungsdossiers für unsere Arzneimittel, mit Fokus auf präklinische (Toxikologie und Sicherheit) und klinische DokumentationErarbeitung der entsprechenden Dokumentationen im Rahmen...

Locations: Switzerland (optional in Germany, Slovakia, Singapore, USA)Contract: PermanentCompany and job overviewARCONDIS is a global consulting company with an exclusive focus on the healthcare and life science industries, managing challenges and solving problems for our clients in compliance, business processes, information technology, and digital...

Présentation: Workload: 80 - 100% Place of work: Fällanden, Switzerland Department: Quality and Regulatory Affairs Start of contract: Immediately or by agreement Responsabilités: - Team member in a team of 5 Regulatory Affairs professionals, positioned in several countries, with Production Sites close to Zurich CH (manufacturer site), Karlsruhe GER...