Local Regulatory Specialist

**Description**: The Sr. Regulatory Affairs Specialist works under mínimal supervision supporting cross functional teams with regulatory strategy and execution of Inari devices and modifications focused on countries Outside the United States (OUS), including but not limited to the European Union (EU), United Kingdom (UK), Middle East,...

**MKS Instruments Deutschland GmbH*** Specialist Regulatory Affairs (f/m/d) - Berlin- Vollzeit- Feste AnstellungMKS in Berlin is looking for a **Specialist Regulatory Affairs (f/m/d)**: In your role as Specialist Regulatory Affairs (f/m/d) at Atotech Deutschland GmbH you are responsible for all aspects of Global Regulatory Affairs such as for the...

**MKS Instruments Deutschland GmbH*** Specialist Regulatory Affairs (f/m/d) - Berlin- Vollzeit- Feste AnstellungMKS in Berlin is looking for a **Specialist Regulatory Affairs (f/m/d)**: In your role as Specialist Regulatory Affairs (f/m/d) at Atotech Deutschland GmbH you are responsible for all aspects of Global Regulatory Affairs such as for the...

Get off to a flying start as a Regulatory Affairs Special ist! Our friendly colleagues in Berlin also have the right job for you: we are currently looking for a Regulatory Affairs Specialist on behalf of our business partner. We are opening the door to this interesting position in the pharmaceutical industry for you! Apply online and look forward to...

**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...

**Requisition Number** **6512** **Employment Type***: **Regular** **Who we are** We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with...

August Research, An Everest Clinical Research Company, is looking for a contractor Regulatory Associate to support our ongoing projects in Germany. This is a freelance position, for a candidate with at least 3 years of experience in the Regulatory field of Clinical Trials. Job responsibilities will include supporting the Regulatory Manager in preparing...

August Research, An Everest Clinical Research Company, is looking for a contractor Regulatory Associate to support our ongoing projects in Germany. This is a freelance position, for a candidate with at least 3 years of experience in the Regulatory field of Clinical Trials. Job responsibilities will include supporting the Regulatory Manager in preparing...

Die Aurora Europe GmbH, mit Hauptsitz in Berlin, ist eine Tochtergesellschaft der börsennotierten Aurora Cannabis Inc., einer der weltweit größten und führenden kanadischen Unternehmen in der Herstellung und dem Vertrieb von Medizinal-Cannabis. Aurora ist seit 2015 Marktführer auf dem deutschen Medizinal-Cannabis-Markt. In Europa ist das Unternehmen...

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific...

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific...

LOCATION- Berlin, Hamburg, Kassel, Germany- STARTING DATE- Next possible starting date- CONTRACT TYPE- Permanent- DEPARTMENT- Carbon Management & Hydrogen- WORKING HOURS- Full-time- REFERENCE CODE- 964- What you can expect- What you can expect- What you can expect - text- You work in a dedicated team in a dynamic market environment. The general...

Der Local Master Data Specialist (LMDM), berichtet an den Head Supply Chain /Market Opeartions, Berlin und ist für das komplette Preismanagement innerhalb von SAP für die Vertriebsorganisationen in Deutschland, Österreich und der Schweiz sowie die Kundenstammdatenerstellung im MDG-Tool für die DACH-Länder verantwortlich. Dazu gehören unterstützende...

**More specifically, you will**: - Establish and monitor the regulatory reports submission process in order to meet compliance requirements within the regulatory reporting calendar. - Design and perform quality assurance controls, KPIs and reconciliation rules that will ensure the accuracy and consistency of the regulatory reports produced. - Ensure reports...

Regulatory Affairs Experte - Lebensmittel / Kosmetik - Freiberuflich Titel und Abteilung: Regulatory Affairs Spezialist (Recht, Toxikologie, Lebensmittel und Kosmetik) Verantwortungsbereich:Regulatory Affairs (Recht, Toxikologie, Lebensmittel und Kosmetik) PrüfberichterstellungKundenspezifikationenProbenbeurteilungKontakt mit Kunden, Handelshäusern,...

Meditrial is a full-service clinical research organization (CRO) dedicated to clinical trial conduct, medical education, regulatory affairs and market access. Our offices are located in Germany, Italy, Switzerland, UK, United States and our teams rely on digital tools to work collaboratively to achieve shared goals. Since 2008, Meditrial delivers...

Meditrial is a full-service clinical research organization (CRO) dedicated to clinical trial conduct, medical education, regulatory affairs and market access. Our offices are located in Germany, Italy, Switzerland, UK, United States and our teams rely on digital tools to work collaboratively to achieve shared goals. Since 2008, Meditrial delivers...

Werden Sie Teil unseres Teams in **Berlin** und unterstützen Sie uns als **Senior Specialist - Regulatory Reporting (w/m/d)**: **Wir bieten facettenreiche Aufgaben**: - Erarbeitung des fachlichen IT-Designs und Schnittstellenbeschreibungen auf Basis regulatorischer und weiterer bankfachlicher Vorgaben - Übersetzung von Fachanforderungen in passende...

**Description** **More specifically, you will**: - Establish and monitor the regulatory reports submission process in order to meet compliance requirements within the regulatory reporting calendar. - Design and perform quality assurance controls, KPIs and reconciliation rules that will ensure the accuracy and consistency of the regulatory reports...

Are you a freelance Medical Device Regulatory Affairs Specialist located in Germany or Switzerland? Do you enjoy working on different projects throughout the year? This may be the opportunity for you! My client is seeking Regulatory Affairs professionals for multiple projects running throughout Germany and Switzerland. The projects are running from 1...