Regulatory Documents Jobs in Germany

Trilogy Writing & Consulting AnIndegeneCompany is a specialized medical writing company that prepares regulatory documentation for the international pharmaceutical industry. We have a vacancy inGermany (hybrid/remote)for a:Resource CoordinatorforMedical Writing(Full time) (f/m/d)Due to continued gro...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activities.Ho...

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 colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and...

You will lead and represent the Drug Product (DP) team for a product and being responsible for defining and executing the activities of drug product development lifecycle management and the technical-scientific support of the commercial production according to the latest state of science and technol...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob Description2 Year Fixed Term contractAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the wo...

The job that makes possibilities real in patients lives. And yours.The job that helps you get ahead in life. Moving mountains together.Welcome to AbbVie! As part of an international company with 48000 employees worldwide and around 3000 employees in Germany you will have the opportunity of addressin...

The job that makes possibilities real in patients lives. And yours.The job that helps you get ahead in life. Moving mountains together.Welcome to AbbVie! As part of an international company with 48000 employees worldwide and around 3000 employees in Germany you will have the opportunity of addressin...

At 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 healthcare journey. Guided by our vision - Creating a future wort...

The central Legal & Compliance team at Miele currently consists of 26 dedicated employees and acts as a reliable business partner for all operational units central functions international locations and management in all legal matters. To strengthen international cooperation with in-house legal colle...

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 colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and...

Joining AbbVie you will be leading a group of highly skilled Technical Leads who oversee and represent all aspects of parenteral Drug Product commercial support and late-stage development including formulation primary packaging and manufacturing process as well as playing a translational role to the...

The Global Product Safety Science Lead (GPSSL) is responsible to strategically lead the Safety Science activities for assigned Sobi products. The GPSSL leads the safety science engagement throughout the product lifecycle including the development and maintenance of the clinical safety profile of the...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAssistant CRA - Germany2 Year Fixed Term contractAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our c...

Join Our Team and Drive Clinical Research Success!At Fortrea we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist you will play a pivotal role in coordinating site start-up activities managing essential documents and ensuring regulatory s...

Including but not limited to the following:Shape and develop the clinical development plans while adhering to the highest scientific and ethical standardsDesign conduct and report Sobi-sponsored studies in close collaboration with the rest of the clinical development team the clinical study teams re...

As Overarching Project Lead you are leading a group of highly skilled QRM experts and defining and aligning global cross-functional strategies regarding QbD and QRM development approaches. Furthermore your are representing the Drug Product (DP) team for a specific project and are responsible for act...