Jurist:in Regulatory Affairs

Are you a fluent German speaker with expertise in regulatory affairs? Do you have a passion for navigating the complex world of pharmaceutical regulations in Germany, Switzerland, and the EU? We are seeking a talented and experienced Regulatory Affairs Consultant to join our dynamic team! The role can be home or office based in various European...

Beschreibung: We make it GmbH is a nationally active company in Switzerland with a high level of expertise in the field of personnel services thanks to many years of successful experience. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We at it GmbH set the highest...

Beschreibung: We make it GmbH is a nationally active company in Switzerland with a high level of expertise in the field of personnel services thanks to many years of successful experience. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We at it GmbH set the highest...

CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, haematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Global Regulatory Affairs...

Are you a fluent German speaker with expertise in regulatory affairs? Do you have a passion for navigating the complex world of pharmaceutical regulations in Germany, Switzerland, and the EU? We are seeking a talented and experienced Regulatory Affairs Consultant to join our dynamic team!The role can be home or office based in various European locations.Key...

Finance Analyst in Global Regulatory AffairsGlobal Regulatory Affairs Finance AnalystWe have a very exciting open position as a Global Regulatory Affairs Finance Analyst with one of our pharmaceutical clients in Bern.Position: Affairs Finance Analyst in Global RegulatoryStart: asapDuration: 6 months with option for extensionLocation: Bern, Hybrid...

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 Unternehmen...

Beschreibung: We make it GmbH is a company operating nationally in Switzerland, which has a high level of competence in the personnel services sector thanks to many years of successful experience. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We make it GmbH...

We make it GmbH is a nationally active company in Switzerland with a high level of expertise in the field of personnel services thanks to many years of successful experience. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We at it GmbH set the highest standards for...

We make it GmbH is a company operating nationally in Switzerland, which has a high level of competence in the personnel services sector thanks to many years of successful experience. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We make it GmbH places the highest...

Do you want to work in a global team and support worldwide registrations for Albumins? The Global Regulatory Affairs CMC Scientist is part of a global team of eight responsible for over 150 Albumins licenses in almost 100 countries worldwide. Albumin is manufactured at four CSL Behring sites and contributes significantly to the companies’ revenue. The...

**My duties** - Maintenance of the content of relevant parts of the regulatory dossiers. - Preparation, revision and review of Module 2.3, Module 3, required facility and equipment information and related documents for new product registrations (e.g. MAAs, BLAs)and lifecycle submissions - Provide timely and high quality answers to CMC-related questions from...

The Dolder Group is a family-owned international company headquartered in Switzerland, offering chemical specialties, thermoplastic granules, and innovative environmental solutions. With a consultative approach and a global network of partners, we support our clients in enhancing their competitiveness, addressing the demands for sustainability and growth.For...

CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions. CSL Behring is committed to delivering medicines that improve their lives.With operations in 35+ nations and ~ 30,000 employees worldwide, CSL is inspired to develop and deliver...

Veranex is the leading service provider for medtech companies. Our global team of experts help clients anticipate challenges and find solutions throughout the development and commercial lifecycle. Together, we accelerate new technologies to market and improve patient outcomes. **About This Role**: We are seeking an experienced Vice President of Regulatory &...

This role’s primary responsibility is to advance the regulatory science and policy field, to monitor, anticipate and provide strategic analyses of t; he European regulatory environment, and to actively participate in the shaping of the regulatory science and policy field in collaboration and alignment with the Head of Global Regulatory Science & Policy and...

**Deine Verantwortung**: - Sie leiten und führen personell den Bereich QM / RA mit drei Mitarbeitenden. - Sie sind verantwortlich für die Leitung des Qualitätsmanagementsystems nach EN ISO 13485, MDR, FDA 820 und GMP. - Im Rahmen der PRRC sind Sie zuständig für die Prüfung der Konformität der Medizinprodukte, die technische Dokumentation (auch deren...

For our location in Bern, we are looking for a **Global Regulatory Affairs CMC Manager (100%) (M/F/d)** **Main Responsibilities and Accountabilities**: - As a Change Control Expert, the position holder is accountable for the timely regulatory assessment of CMC changes, technical changes related to facility and equipment and/or plasma changes in the Global...

PositionWir suchen einen Medizinprodukte-Experten/ eine Medizinprodukte-Expertin, der/die sich in einem herausfordernden und dynamischen Umfeld einsetzt, um die Verfügbarkeit und Versorgungssicherheit von Medizinprodukten in der Schweiz zu gewährleisten.BeschreibungIn dieser Rolle werden Sie Teil eines interdisziplinären Teams sein, das sich auf die...

Job Title: CMC Quality By Design ExpertAbout Us: At Consultys, we are a leading consulting firm dedicated to helping pharmaceutical and biotechnology companies navigate the complex world of Quality by Design (QbD) and regulatory affairs.About the Role:We are seeking an experienced Quality by Design Consultant who can lead our client's CMC (Chemistry,...