Congratulations! Your Premium Role is active for one month—apply to unlimited jobs and boost your career!

Full Name
Please upload CV in pdf format only.
Ainult üks fail. | 256 MB limiit. | Lubatud tüübid: pdf.
Please write some lines about this question.
Please write some lines about this question.
Please write some lines about this question.
Please write some lines about this question.

 

About us:
As part of your job, you will work in the Medical & Scientific Affairs division of the Regulatory Affairs department. The Regulatory Affairs department (drug approval) ensures the market access of new drugs and the maintenance of existing drug approvals in Germany in Europe-wide cooperation with specialist departments from research and production. This also includes the technically correct labeling of medicinal products for the German market. One focus of this activity is the coordination and timely submission of applications to the higher federal authority. You will support the regulatory affairs officers in the planning and implementation of projects; you will carry out small projects independently with the support of the regulatory affairs officers. 
Job description:
Collaboration in the preparation, creation and processing of national variations on pharmaceutical quality and changes to the informative texts Checking technical and package leaflet artwork for print approval Comparing list extracts with database entries for completeness checks as part of internal quality control and updating database entries if necessary Technical revision of product monographs Completion of approval masks Supporting compliance checks of chemical-pharmaceutical documentation and updating it Support in responding to service requests Research activities, archive maintenance and paper filing Insight into related subject areas Requirements & qualifications You have completed or will soon complete the 2nd stage of pharmaceutical training (2nd state examination in pharmacy) A keen interest in pharmaceutical processes In addition to your knowledge in the classic areas of pharmacy, you would like to deepen your knowledge in the area of drug approval and drug information Confident use of standard software (MS Office) Independent working style and motivation with a strong sense of initiative Very good communication skills, strong German and English writing and speaking abilities.
Our benefits:
An international working environment in which you can develop your talents and realize ideas and innovations together in a competent team An individual and structured induction to your new tasks You can shape your personal career path at Sanofi and we will support and accompany your professional and personal development in a targeted manner As a globally successful, growing healthcare company, Sanofi offers a variety of career paths, including global ones Pursue Progress. Discover Extraordinary. Advancing science is our purpose. Every day. Always. But progress doesn't happen without people - people from different backgrounds, in different places, in different roles—all united by one thing: the desire to create miracles. At Sanofi, we are committed to equal opportunities for all, regardless of race, color, religion, gender, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Find out more about our programs for more diversity, equality, and integration in our ALL IN video and at www.sanofi.de/Karriere! Become part of our great team! Diversity and inclusion are fundamental to Sanofi's operations and are ingrained in our core values. We understand that in order to fully benefit from diversity, we must practice inclusive leadership, create a work environment where differences are valued, and use those differences to improve the lives of our clients, coworkers, and patients. We value and honor the variety of our people, their histories, and their experiences, and we provide everyone with the same opportunities. Similar jobs (2168) Sanofi-Aventis Germany GmbH Pharmacy Intern in Medical Scientific Affairs/Regulatory Classics Compliance for November 2025 Berlin (2168) Sanofi-Aventis Deutschland GmbH Sanofi-Aventis Germany GmbH Pharmacy Intern in Medical & Scientific Affairs/Regulatory Classics & Compliance for November 2025 Berlin, Germany Sanofi-Aventis Germany GmbH Sanofi-Aventis Germany GmbH Pharmacy Intern in Medical & Scientific Affairs/Regulatory Classics & Compliance for November 2025 Berlin, Germany Sanofi-Aventis Germany GmbH Sanofi-Aventis Germany GmbH Pharmacy Intern in the field of Regulatory Affairs Artwork for November 2024 Berlin Sanofi-Aventis Germany GmbH (2168) Sanofi-Aventis Deutschland GmbH Pharmacy Intern in the area of Medical Scientific Affairs/Regulatory Classics Compliance for May 2025 Berlin (2168) Sanofi-Aventis.

info@danaher.com
Danaher Corporation
10808
10808
10808