Regulatory & Clinical Affairs Specialist

Regulatory & Clinical Affairs SpecialistExperts in developing devices for minimally invasive surgery and imaging, my client in their growth phase has partnered with me to find the right fit! We are seeking a dedicated professional with grit to manage the registrations and compliance efforts for their award-winning products in the EU & US. This hybrid...

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...

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...

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...

Your missionYour Mission: You will be responsible for the development and upkeep of regulatory documentation to ensure compliance with global standards. Key tasks include:Develop and execute regulatory strategies aligned with business objectivesCreate, submit, and maintain regulatory documentation, including technical files and submissions required for...

Your missionYour Mission: You will be responsible for the development and upkeep of regulatory documentation to ensure compliance with global standards. Key tasks include: Develop and execute regulatory strategies aligned with business objectivesCreate, submit, and maintain regulatory documentation, including technical files and submissions required for...

Your missionYour Mission: You will be responsible for the development and upkeep of regulatory documentation to ensure compliance with global standards. Key tasks include:Develop and execute regulatory strategies aligned with business objectivesCreate, submit, and maintain regulatory documentation, including technical files and submissions required for...

**INNOMEDICA IST EIN JUNGES NANOTECH-UNTERNEHMEN** mit ca. 50 Mitarbeitenden, einer Reihe erfolgversprechender Medikamente in präklinischer und klinischer Entwicklung sowie eigener Reinraum-Produktion. Die Pipeline basiert auf einem firmeneigenen liposomalen Transportsystem und umfasst insbesondere Anwendungen in den Bereichen Onkologie (schonende...

Your missionYour Mission: You will be responsible for the development and upkeep of regulatory documentation to ensure compliance with global standards. Key tasks include:Develop and execute regulatory strategies aligned with business objectivesCreate, submit, and maintain regulatory documentation, including technical files and submissions required for...

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,...

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...

**Purpose**: Lead counsel responsible for providing and coordinating specialist legal advice on safety and pharmacovigilance matters in CSL’s key jurisdictions, and strategic and specialist legal advice on regulatory matters. **Responsibilities**: - Provide specialist legal advice to CSL’s Global Regulatory Affairs (GRA) and Global Clinical Safety &...

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...

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. -...

**INNOMEDICA IST EIN JUNGES NANOTECH-UNTERNEHMEN** mit ca. 50 Mitarbeitenden, einer Reihe erfolgversprechender Medikamente in präklinischer und klinischer Entwicklung sowie eigener Reinraum-Produktion. Die Pipeline basiert auf einem firmeneigenen liposomalen Transportsystem und umfasst insbesondere Anwendungen in den Bereichen Onkologie (schonende...

**INNOMEDICA IST EIN JUNGES NANOTECH-UNTERNEHMEN** mit 50 Mitarbeitenden, einer Reihe erfolgversprechender Medikamente in präklinischer und klinischer Entwicklung sowie eigener Reinraum-Produktion. Die Pipeline basiert auf einem firmeneigenen liposomalen Transportsystem und umfasst insbesondere Anwendungen in den Bereichen Onkologie (schonende...

**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...

**Position Purpose**: The Dir., Sr. Global Regulatory Lead, Hematology TA, is a member of a GRA GPS Therapeutic Area and contributes to the vision and goals for Global Regulatory Affairs (GRA) as: - ** GRA** Representatives** **on Product/Project Strategy Teams (PSTs), key Delivery Teams (e.g., Clinical Development Teams [CDTs], Safety Management Teams...

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...