773 days ago on chemiepharma.ch

International Regulatory Affairs

Chemie-Pharma AG

  • Sector
  • Employment type
  • Position

 Please refer to JobSuchmaschine in your application

International Regulatory Affairs

Ref. 2025 International Regulatory Affairs


• In Zurich based pharmaceutical company focusing on Gynaecology and Dermatology.

Products are available in Europa, Asia, Middle East and Centrals America, and the company

is part of the Health Care Business Unit of DKSH.


• Handling all regulatory projects in the European Union and Eastern Europe. Within this region

the person will be responsible for new applications, variations, renewals and daily

communications with external agents and the corresponding Health Authorities. Additionally,

the person will be part of the registration dossier team to compile and update the master and

country-specific files according to the newest regulation. For this task, it would be an

advantage to have experience in writing clinical regulatory documents (expert reports,

summaries, study reports). Main requirements: Scientific, pharmaceutical or medical university

degree; 3 to 5 years experience in Regulatory Affairs; Experience in compiling registration

dossiers acc. NTA 98 or CTD; Ability to write expert reports / overviews (preferably clinical);

Excellent written and verbal communication skills; Capacity to operate successfully within a

team environment as well as an individual performer

• Arbeitsregion: ZH

• Bereich/Funktion: Regulatory

• Jobsprache: Deutsch

• Beschäftigungsart: Vollzeit


• Chemie-Pharma AG

• Blegistrasse 25

• 6340 Baar

• Tel. Zentrale AG ++41 056 648 25 75

• E-Mail: info@chemiepharma.ch