Regulatory Affairs Specialist – Medical Devices

**This is where you save and sustain lives** At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in...

**This is where you save and sustain lives** At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in...

Join us today and make a difference in people's lives! Regulatory Affairs Specialist (M/F/d) Position Summary The Regulatory Affairs Specialist implements and conducts the activities required to obtain and maintain regulatory clearance for the company's medical device products. General Responsibilities - Participating on project teams to provide input to...

Proclinical is on the lookout for a Senior Regulatory Affairs Manager. In this role, you will be responsible for developing and implementing regional regulatory strategies for the development, registration, commercialisation, and lifecycle management of assigned products/projects in the EMEA region. You will also manage affiliate level local Regulatory...

Proclinical is seeking a Senior Medical Affairs Manager who will be responsible for developing and executing Medical Affairs strategy for a region within International, focusing on existing and new distributor markets. This role involves working closely with distributor companies, cross-functional partners, and Medical Affairs colleagues to ensure the...

Proclinical is seeking a Senior Medical Affairs Manager who will be responsible for developing and executing Medical Affairs strategy for a region within International, focusing on existing and new distributor markets. This role involves working closely with distributor companies, cross-functional partners, and Medical Affairs colleagues to ensure the...

**This is where you save and sustain lives** At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in...

Linde GmbH, Gases Division Regulatory Affairs Specialist Medizinische Gase (m/w/d) Unterschleißheim, Deutschland (req12198) **Hier sind Sie in Ihrem Element** - Als Regulatory Affairs Specialist bei QRA stellen Sie sicher, dass erforderliche lokale Zulassungs-Aktivitäten für als Arzneimittel eingestufte medizinische Gasprodukte identifiziert, geplant,...

**This is what you will do**: The Medical Advisor Metabolics is a member of the Medical Affairs Team and will provide scientific and medical leadership especially for metabolic indications in establishing an in depth understanding of the relevant medical landscape in relation to relevant disease states and Alexion products. The Medical Advisor Metabolics is...

Hobson Prior are currently seeking for a RA Project Lead - Medical Devices (Manufacturing) to join a pharmaceutical organisation on a contract basis with the ability to work remotely from anywhere in Europe, apart from Belgium. Our client is focused on producing a healthier society. Please note that to be considered for this role you must have the right to...

Responsibility for regulatory strategy to support the development of biomarkers, companion diagnostic tests and other devices to enhance the value of our oncology pharmaceutical products. The job holder provides innovative approaches to resolve complex regulatory issues and increase speed to patients. **Roles & Responsibilities**: - CDx development:...

Aufgaben Assessing technical documentation, product dossiers and test results of production batches of in-vitro diagnostic products, most high-risk products as part of product conformity assessments according to the requirements of the IVDR Preparing reports included deficiency reports in case of non-conformities according to the requirements of the...

Karo is at an exciting stage in its journey to become a €1 billion European leader in consumer healthcare._ - Our purpose is to deliver better everyday health through smart choices and after a series of exciting acquisitions, we now own a strong portfolio of consumer healthcare brands, including E45, Decubal, Nailner, CCS, Multi-Gyn, Flux, Paracet, Alpha...

Seit 1866 gilt unsere Leidenschaft der Technik und der Sicherheit. Innovationen beeinflussen unser Leben in vielfältiger Weise. Für die Sicherheit von Menschen und der Gesellschaft setzen wir uns jeden Tag aufs Neue ein und schaffen Vertrauen in neue Technologien. Wir sind Teil des Fortschritts. Wir beraten, wir prüfen, wir zertifizieren. Wir handeln aus...

**Position: Regulatory Affairs CMC** **About the Company**: A renowned pharmaceutical consulting firm is currently seeking a Regulatory Affairs CMC expert with a strong background in **small molecules** and pharmaceuticals. This role offers the opportunity to provide expert guidance on regulatory strategies for drug development projects, ensuring adherence...

Otsuka Novel Products GmbH (ONPG) is the global headquarter for a special pharmaceutical business within the Otsuka group. With an international network of 168 subsidiaries and 34,400 employees in 32 countries and regions across Europe, Asia-pacific, America and the Middle East, Otsuka researches, develops, manufactures and markets innovative and original...

Proclinical are recruiting an Associate Director Medical Information Germany for a pharmaceutical establishment. This role is on a permanent basis and is located in Germany. The client is focused on creating, developing and commercialising life-changing solutions for those suffering from severe illnesses. **Responsibilities**: - Uphold core product...

Passion for Innovation. Compassion for Patients. With over 120 years of experience and more than 17,000 employees in over 20 countries, Daiichi Sankyo is dedicated to discovering, developing, and delivering new standards of care that enrich the quality of life around the world. In Europe, we focus on two areas: The goal of our Specialty Business...

Your role Participate in complex project product development with R&D and PM, identify potential clinically relevant issues emerging from (absence of) features and their clinical consequences, define and implement the appropriate clinical evaluation strategy and necessary clinical studies for the product Responsibility for budget and time...

**Job Description**: Für unser Office in München (in einem hybriden Arbeitsmodel) suchen wir aktuell einen **Trainee, Medical Affairs (w/m/d)** **Über die Position** Das Medical Traineeprogramm (Vollzeit) richtet sich an qualifizierte junge Fachkräfte (z. B. MD, MSc, Pharmazeuten oder Doktoranden in Natur - oder Biowissenschaften) aus Hochschulen,...