Regulatory Affairs Manager Pharma Eu/ch

Deine Aufgabe - Der Erfolg unserer Kunden bei der Markteinführung regulierter Produkte ist dein Antrieb. Als Senior Consultant bist Du ein Fachexperte, der interdisziplinäre Teams befähigt. Als inspirierende Führungspersönlichkeit schaffst Du Klarheit über regulatorische Anforderungen und hilfst deinen Kolleg:innen und Kund:innen, pragmatische...

Who we are You enjoy creating and innovating. You never stop striving for better. You take responsibility and you get results. You love being part of a team. Above all, you want your work to matter: Welcome to our world! At Sonova we create sense by bringing sound to life. Our innovative hearing care solutions help millions of people enjoy life’s...

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...

**OBJECTIVE**: - Collaborates to define, develop and sometimes lead regional strategies to maximize regulatory approvals and patient access to meaningful medicines in alignment with program objectives - Provides regional strategic and tactical advice and guidance to teams to achieve timely and efficient conduct of development programs, while maintaining...

Regulatory Affairs Manager (M/F/d) time type: 60%/80%/100% This is what you can look forward to: - Overseeing assigned product portfolio of innovative prescription drugs with complex regulatory background - Handling entire regulatory lifecycle from initial MAAs to line extensions, labeling and CMC variations, renewals, PSUR submissions, etc. - Developing...

**SUMMARY** Responsible for - ** Regulatory Affairs** Obtain and maintain marketing authorizations for products and communication of general regulatory requirements in support of licensing of Takeda’s products **TASKS AND RESPONSIBILITES** - Manage **MA lifecycle maintenance** for a defined product portfolio, inclusive local impact assessments of global...

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

CSL Vifor is currently undergoing unprecedented growth and portfolio expansion within rare diseases, Nephrology and Cardiorenal therapeutic areas. A permanent global position in the Global Regulatory Affairs Labelling team has arisen. Which can be based at any of our CSL R&D Hubs (Maidenhead UK, Amsterdam, NL, Bern, CH, Zurich, CH, KOP, PA or Waltham,...

**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our...

Regulatory Affairs Manager (M/F/d) 80-100% This is what you can look forward to: - Overseeing assigned product portfolio of innovative prescription drugs with complex regulatory background - Handling entire regulatory lifecycle from initial MAAs to line extensions, labeling and CMC variations, renewals, PSUR submissions, etc. - Developing of submission...

**People First** - At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. **Our people are the heart of Takeda**. Are you a strategic and visionary leader with a strong background in regulatory affairs within the...

**People First** - At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. **Our people are the heart of Takeda.** Our team is growing and for this we need bright minds with creativity and flexibility - what talent do...

**Responsibilities**: - Handle integrated quality systems with ISO 13485/9001/14001/45001/17025, as well as ISO 50001 would be advantageous. - You will manage EU IVDR roll out in a global analytical instrumentation corporation - from approval process to daily improvements and managing audits. - Guide and develop a team of around 20 professionals within 3...

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as an **Associate Director, Global Regulatory Affairs Development GI** to be based in Zurich, Switzerland. **Here, you will be a vital contributor to our inspiring, bold mission.** **OBJECTIVE**: - Defines, develops and leads global...

**People First** - At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. **Our people are the heart of Takeda.** Our team is growing and for this we need bright minds with creativity and flexibility - what talent do...

If you find science, speed, and success exhilarating, you have come to the right place. Novavax, Inc (Nasdaq:NVAX) is a biotechnology company that creates transformational vaccines that address some of the world’s most pressing infectious diseases. We have more than a decade of experience contending with some of the world’s most devastating diseases,...

Our client a global pharmaceutical company specializing in rare diseases, Nephrology and Cardiorenal therapeutic areas is looking to appoint a Regulatory Affairs Labelling manager in their Zurich offices. This is an excellent opportunity to gain global experience within RA labelling in a high performing team at a time when multiple new drug development...

Our team is growing and for this we need bright minds with creativity and flexibility - **what talent do you have?** **OBJECTIVE**: - Effectively communicates the regulatory strategies, submission plans and timelines; assessment of the likelihood of success of the regulatory strategies and impact assessments of trends, regulations and changes related to...

agap2 is a dynamic and rapidly growing company and employs more than 6000 people in ten European countries. With more than 200 employees in Switzerland, we are specialized in Life Science, MedTech, Pharma, BioTech, etc. Our offices in Switzerland are located in Basel, Zürich, and Lausanne. agap2 works successfully in all areas of the product life cycle,...

agap2 is a dynamic and rapidly growing company and employs more than 6000 people in ten European countries. With more than 200 employees in Switzerland, we are specialized in Life Science, MedTech, Pharma, BioTech, etc. Our offices in Switzerland are located in Basel, Zürich, and Lausanne. agap2 works successfully in all areas of the product life cycle,...