Position overview

The export team is looking for a dual role member to spearhead our efforts in the quality management and export fields. We are looking for a member that is passionate about working in a multinational environment and could operate and communicate efficiently with our customers, distributors and subcontractors around the world.

The position is located in our headquarters: Dellenbodenweg 8, 4452 Itingen, Switzerland and the team is looking to fill it immediately

Key Qualifications

  • Varied pharmaceutical background (Education & Professional Experience)
  • A sharp knowledge of the regulatory constraint in the pharmaceutical field and a good ability to manage products registrations and releases in different countries around the world
  • Being fluent in English, Arabic and French in order to conduct workshops and oral and written discussions and communicate with our subcontractors, customers and distributors
  • Ability to work efficiently with the Microsoft Office Suite (Word, Excel and PowerPoint)
  • A sharp knowledge of the quality verification and validation workflow in order to validate the product batches intended to export

The main tasks related to this position are:

  • Conducting the process of the product registration in different countries
  • Preparation of submission regulatory files to the authorities for the registration of our products
  • Follow-up of submissions
  • Ensure the quality control of products intended for export.
  • Management of corporate requests concerning registered files
  • Preparation and submission of special request (renewals of registrations and marketing authorizations, etc.)
  • Participation in strategic registration discussions (within the department, logistics, marketing, etc.)
  • Updating or drafting of internal procedure
  • Continuous updating of the company databases
  • Serve as the regulatory export representative with the customers, distributors and subcontractors

 

Other skills

  • Critical mind
  • Accuracy and sense of organization and analysis
  • Team spirit
  • Great communication skills

Education & Experience

  • MS or PhD in Pharmaceutical Science or related fields
  • A previous experience in pharmaceutical industry regulatory affairs is required

Please send your application documents with photo to

Danny Chandler

Tentan AG
Dellenbodenweg 8
4452 Itingen

Fax +41 (0)61 975 05 12