Regulatory Affairs Jobs in Czech Republic

Career CategoryRegulatoryJob DescriptionThe Senior Associate in Regulatory Affairs supports country regulatory activities for the development registration and lifecycle management of all Amgen molecules. Contract type: Amgen Paid Temp - contract for 1 year fulltime jobReports to: Associate Director...

Job DescriptionThe Senior Regional Submissions Planner will work within our Global Regulatory Affairs and Clinical Safety (GRACS) organization in the Regional Regulatory Operations department (RRO) supporting regional planning activities for the EU EEMEA region while also contributing to cross-regi...

Serving as the primary contact for regulatory authorities and internal stakeholders.Managing Regulatory Affairs including registrations renewals variations and product information updates.Overseeing Pharmacovigilance activities locally and ensuring compliance with global PV requirements.Ensuring GDP...

Job DescriptionThe Specialist Regional Submissions Planner will work within the our Global Regulatory Affairs and Clinical Safety (GRACS) organization in the Regional Regulatory Operations department (RRO) supporting regional planning activities for the EU EEMEA region while also contributing to cr...

Some careers open more doors than others.If youre looking for a career that will unlock new opportunities join HSBC and experience the possibilities. Whether you want a career that could take you to the top or simply take you in an exciting new direction HSBC offers opportunities support and rewards...

Medical Advisor Oncology (Breast Cancer) MAT Cover Contract Czech Republic Diverse Minds. Bold Disruptors. Meaningful Impact.AstraZeneca is a global science-led patient-focused biopharmaceutical company that focuses on the discovery development and commercialization of prescription medicines for s...

Job DescriptionJob Description: Seeking a full-time Business System Associate Director for the Labeling Operations area within the GRACS Regulatory Innovation & Information Management organization.Primary area of responsibilities will include:Manage and lead Business Analysts for complex data analyt...

Job Description SummaryJob description summary#LI-HybridJob Posting Title: SSO Study Start-Up ManagerLocation: Prague Czech RepublicThe SSO Study Start-Up (SSU) Manager is accountable for study planning SSU activities and activation deliverables of assigned projects in compliance with Novartis proce...

No Relocation Assistance OfferedJob Number#173263 - Prague Prague Czech RepublicWho We AreColgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care Personal Care Home Care Skin Care and Pet Nutrition. Our products are trusted in more ho...

Medical Advisor Oncology (Gynaecological Cancer) Czech Republic Diverse Minds. Bold Disruptors. Meaningful Impact.AstraZeneca is a global science-led patient-focused biopharmaceutical company that focuses on the discovery development and commercialization of prescription medicines for some of the...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our team to enable our customers to make the world healthier cleaner and safer.DESCRIPTIONDivision: Materials &...

Cluster Expert for Medical Device Regulatory Affairs and VigilanceAt Fresenius Medical Care we are the global leader in kidney care committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality innovative products services and care across the entire...

The role of Contracts and Systems Manager CEERJ is to provide support to the teams in the CEERJ region in relation to preparing reviewing managing and overseeing contracts and contractual processes including HCC templated agreements and other third-party vendor agreements as well as managing and dev...

Job DescriptionWe invite you to join our mission of advancing the prevention and treatment of diseases. The purpose of Global Labeling is to drive labeling strategy and ensure high-quality and compliant labeling documents which provide instructions for the safe and effective use of products for pati...

Job DescriptionThe Regional Dossier Publisher (RDP) will work within the Global Regulatory Affairs and Clinical Safety (GRACS) organization in the EUEEMEA Regulatory Operations (RRO-EUEEMEA) Team.The RDP is responsible for publishing key regulatory submissions in the region and supporting the publis...

Job DescriptionThe Regional Dossier Publisher (RDP) will work within the Global Regulatory Affairs and Clinical Safety (GRACS) organization in the EUEEMEA Regulatory Operations (RRO-EUEEMEA) Team.The RDP is responsible for publishing key regulatory submissions in the region and supporting the publis...

Job DescriptionThe Regulatory Affairs Operations will support regional activities associated with the implementation and support of Global Regulatory Affairs Compliance and Safety (GRACS) Digital Strategy projects and systems. With some understanding of regulatory affairs and supporting business pro...

Job DescriptionThe Regulatory Affairs - System Process & Innovation will support regional activities associated with the implementation and support of Global Regulatory Affairs Compliance and Safety (GRACS) Digital Strategy projects and systems. With some understanding of regulatory affairs and sup...

Job DescriptionThe Regulatory Affairs - System Process & Innovation will support regional activities associated with the implementation and support of Global Regulatory Affairs Compliance and Safety (GRACS) Digital Strategy projects and systems. With some understanding of regulatory affairs and sup...

Job DescriptionThe Regulatory Affairs - System Process & Innovation will support regional activities associated with the implementation and support of Global Regulatory Affairs Compliance and Safety (GRACS) Digital Strategy projects and systems. With some understanding of regulatory affairs and sup...