Regulatory affairs Jobs in Schweiz

Die Iscador AG ist ein Pharmaunternehmen, das Präparate für die integrative Behandlung von Krebserkrankungen herstellt, wissenschaftlich erforscht und weltweit vertreibt. Die Misteltherapie ist seit Jahrzehnten ein bewährter Bestandteil der integrativen Krebstherapie. Unser Ziel ist es, den Einsatz von unseren Produkten in der Onkologie weiter auszubauen. Als Ergänzung für unser Team suchen wir...

Sie sind für die Koordination und Umsetzung der qualitätsrelevanten Aufgaben im Rahmen unseres EN/ISO/QM-Systems verantwortlich und bereiten den relevanten Normenraum für die anderen Abteilungen der Geschäftseinheit für die Umsetzung auf. Ihr Aufgabengebiet beinhaltet: - Unterhalt und Pflege des Qualitätsmanagementsystems - Erstellen der Richtlinien und Qualitätsdokumentation mit den...

Our client is an established, innovation-focused pharmaceutical company with a strong presence in the Swiss market. The organization operates internationally and is active in several therapeutic areas with a clear commitment to high-quality regulatory standards. For their Swiss affiliate, we are currently seeking aRegulatory Affairs Manager (Ref) – Permanent RoleZurich / Fluency in GermanIn this...

You will be a member of the local regulatory affairs and CMC team dedicated to Drug Substance and ADCs/Bioconjugates Business Unit and will support customer activities focusing on Chemistry Manufacturing and Controls (CMC) for Biologics and Chemistry projects. In this very dynamic and hands-on role, you will work collaboratively with the other departments to coordinate the regulatory activities...

Allgemeine Chirurgie und Ästhetik, Ort: St. Gallen / Pensum% Darauf können Sie sich freuen: - Spannende, abwechslungsreiche Tätigkeit mit Freiraum für Ideen und Eigeninitiative - Internationales Umfeld in zukunftsorientierter, innovativer Health Care Branche - Attraktive und flexible Arbeits- und Anstellungsbedingungen Ihr Verantwortungs- und Aufgabenbereich: - Mitarbeit in der Vorbereitung...

Vice President, Communication, Public Affairs and Advocacy, EuropeJoin to apply for the Vice President, Communication, Public Affairs and Advocacy, Europe role at Revolution MedicinesRevolution Medicines is a clinical‑stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS‑addicted cancers. The R&D pipeline comprises RAS(ON) Inhibitors...

Head of Medical Affairs, Europe – GenmabGenmab is an international biotechnology company dedicated to transforming the lives of patients with cancer and other serious diseases through innovative antibody therapeutics. With a 25‑year legacy of science‑driven innovation, Genmab continually develops next‑generation antibody platforms, including bispecific T‑cell engagers, antibody‑drug conjugates...

At Genmab, we are dedicated to building extraordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet...

Overview Reporting to the Head of Government Affairs in the International Region, the Associate Director, Government Affairs & Public Policy, Austria and Switzerland will be responsible for developing and executing Government Affairs & Public Policy initiatives in Austria and Switzerland in alignment with the International GAPP Department and the Austrian and Swiss country leadership teams....

A global medical devices and pharmaceutical company in Basel is seeking a motivated RAQA Assistant to join their Regulatory Affairs & Quality Assurance team. This entry-level position offers structured learning and professional development in regulatory affairs and quality assurance within the life sciences sector. Ideal for graduates or early-career professionals, the role includes supporting...

<< ZURÜCKBEWERBENvon: Sobi The Global Regulatory CMC Lead develops and executes global regulatory CMC strategy for assigned Sobi assets in development prepares CMC sections of IND/IMPD MAA NDA/BLA as well as assesses global filing strategy for post approval changes.The role holder works closely with Global Manufacturing Sciences subject matter experts Quality representatives and cross-functional...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and...

Jobdescription Job Title: SeniorClinical Project Manager, ClinicalOperations Location:Switzerland /UK Entity: ClinicalResearch Unit, Clinical Operations,Pharma Work rate:100 % Contract type:Temporary Desired startdate: ASAP End ofassignment: Jan2027 Summary TheSenior Clinical Project Manager (sCPM), Clinical Operations, isresponsible for the planning, execution, and oversight of...

MANPOWER AG - Your career, our focus!Become part of our network and take advantage of the numerous opportunities!The ManpowerGroup is the world's leading provider of workforce solutions.With our three brands - Manpower, Experis, and Talent Solutions - we support companies in various industries with their recruitment needs. For 75 years, we have been operating in over 75 countries and supporting...

Die Gebro Pharma AG in Liestal BL ist ein inhabergeführtes Pharmaunternehmen mit starkem Fokus auf spezialisierte Arzneimittel. In der Schweiz ist der Bereich Rheumatologie / Schmerz ein zentraler Pfeiler unserer Rx-Aktivitäten und trägt wesentlich zum nachhaltigen Wachstum von Gebro bei. Zur Verstärkung unseres Rx-Marketing-Teams suchen wir per sofort oder nach Vereinbarung dich als Product...

Your main tasks and responsibilities - Responsible for project management of NIS and IIS - Manage the publication processes related to clinical studies conducted by Octapharma - Literature research on Octapharma's products, competitor products and indications thereof for: - Product reviews for submissions to international health-authorities - Response to internal scientific questions - Response...

True to the vision "We drive innovation to improve people's lives", the Hamilton companies have been providing solutions for the health sector sinceWe are an innovative pioneer in the fields of ventilators, automated pipetting, sample management and in the development of process sensors.Hamilton Medical is a leading manufacturer of intelligent ventilators. Whether in ICUs, during emergency rescue...

to lead strategic and operational CMC regulatory activities across product development, clinical submissions, registrations, and lifecycle management. In this role, you will shape global CMC regulatory strategy, ensure compliant execution of submissions and changes, and partner with technical and regulatory teams worldwide. Key Responsibilities: - Drive global CMC strategies for clinical trial...

Die Curaden AG mit Sitz in Kriens bei Luzern ist mehr als nur ein Unternehmen - wir verkörpern eine Vision, ein System und eine Philosophie, die weltweit Massstäbe setzt. Unter unserer Marke CURAPROX revolutionieren wir die Zahnpflege und streben nach nichts Geringerem als einer gesünderen und glücklicheren Gesellschaft. Unser Versprechen "Better health for you" treibt uns an, innovative und...

Sie sind für die Koordination und Umsetzung der qualitätsrelevanten Aufgaben im Rahmen unseres EN/ISO/QM-Systems verantwortlich und bereiten den relevanten Normenraum für die anderen Abteilungen der Geschäftseinheit für die Umsetzung auf. Ihr Aufgabengebiet beinhaltet: - Unterhalt und Pflege des Qualitätsmanagementsystems - Erstellen der Richtlinien und Qualitätsdokumentation mit den...