Regulatory Affairs Associate

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...

Social network you want to login/join with:Regulatory & Clinical Affairs Specialist, BernClient:headcount AGLocation:BernJob Category:OtherJob Reference:17982f88f11aJob Views:5Posted:21.01.2025Expiry Date:07.03.2025Job Description:Regulatory & Clinical Affairs SpecialistExperts in developing devices for minimally invasive surgery and imaging, my client in...

**About SciPro**Spectrum of innovative medical devices calls for expert regulatory guidance. As a key member of the SciPro team, you will be instrumental in ensuring our products meet international standards.This role demands an exceptional individual with expertise in regulatory affairs and clinical management. Key responsibilities include:Developing...

This position focuses on managing and updating regulatory documentation to ensure compliance with international standards. Key responsibilities include:Responsibilities:Designing and executing regulatory strategies that align with organizational objectives.Preparing, submitting, and maintaining essential regulatory documents, such as technical files and...

Job DescriptionThe Global Regulatory Lead (GRL) Consultant is a member of a GRA Global Product Strategy Therapeutic Area and contributes to the vision and goals for Global Regulatory Affairs (GRA) as:Regulatory leaders, who drive development and implementation of innovative, scientifically sound, prospective, global regulatory strategies for product/s,...

Get AI-powered advice on this job and more exclusive features.Direct message the job poster from SciProPrincipal Specialist Consultant at SciPro - Medical Devices & Digital Health across DACHThis position focuses on managing and updating regulatory documentation to ensure compliance with international standards. Key responsibilities...

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...

**Responsibilities**: - Plan, direct, and monitor regulatory affairs activities so the organization has the permits, licenses, certificates, authorizations, and other approvals needed to conduct current and future business activities; and produce, sell, and distribute its goods and services. - Support development of consistent roles and work processes. -...

About the CompanyJanssen Vaccines in Bern (Switzerland) belongs to the Janssen Pharmaceutical Companies of Johnson & Johnson. We are an organization of over 40,000 professionals working passionately to prevent, treat, cure, and stop some of the most devastating and complex diseases of our time.Our Team:About 400 people of over 25 nationalities work together...

Our customer is a leading Swiss SME and developer of cutting edge High-Tech Medical Device technology. A disruptor in their field with a strong Engineering core originating at Bern University, though now employing some of the brightest minds in Electronics, Mechatronics, physics and Software development. We have been tasked to identify and recruit a...

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...

**Arbeitspensum: 80-100%** **Ihre Aufgaben**: - Innerhalb eines kleinen Teams sind Sie mitverantwortlich für die GMP Compliance und Zulassungskonformität unserer tiermedizinischen Produkte sowie die GDP Compliance der Lieferkette. - Zudem wirken Sie mit bei allen regulatorischen Zulassungsaufgaben entsprechend den gesetzlichen Richtlinien und den...

We are looking for a Chemical Affairs Specialist with expertise in regulatory affairs to join our team at Dolder Group.Key ResponsibilitiesManage and maintain accurate records of regulatory documents and certifications.Monitor and report on regulatory changes affecting our operations.Collaborate with colleagues to ensure compliance with relevant laws and...

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...

Social network you want to login/join with:Regulatory and Clinical Affairs Specialist, BernClient:CASCINATION AGLocation:BernJob Category:OtherJob Reference:0e25671dc31eJob Views:7Posted:21.01.2025Expiry Date:07.03.2025Job Description:Your missionYou will be responsible for the development and upkeep of regulatory documentation to ensure compliance with...

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...

**Unternehmenspräsentation** AIR LIQUIDE** ist ein Weltmarktführer bei Gasen, Technologien und Services für Industrie und Gesundheit. Mit rund 66.400 Mitarbeitern in 75 Ländern versorgt Air Liquide mehr als 3,8 Millionen Kunden und Patienten. Sauerstoff, Stickstoff und Wasserstoff sind kleine Moleküle von grundlegender Bedeutung für das Leben, für die...