Specialist Regulatory Affairs 100% (w/m)
Bachem Holding AG
Bubendorf; Switzerland
vor 32 Tg.

Your responsibilities

We look for someone who excels at writing and explaining scientific facts. You will compile regulatory dossiers for our products for customers and / or Health Authorities worldwide.

This involves participation in development project teams, close cooperation with other departments and customers, and responding to Health Authority questions.

You will be solely responsible for various projects including maintenance of the regulatory dossiers, customer support, and review of GMP documents for compliance with regulatory dossiers and relevant guidelines.

Your qualifications

  • Master or PhD in live sciences, who allows you to explain the chemical and analytical background of our products to reviewers and customers
  • You are used to working on your projects independently while still understanding yourself as part of a team
  • As a precise worker, you strive to deliver high-quality results and you benefit from good organizational skills to master complex tasks and to keep deadlines
  • Excellent communication skills in German and English
  • You interact effectively and convincingly with internal and external customers
  • Desirable

  • Experience with Drug Regulatory Affairs and knowledge of GMP
  • We offer

    We offer you a new challenge joining a motivated team in an internationally renowned company, and excellent terms and conditions.

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