In this role, you will support the organization by handling administrative tasks, preparing reports, and ensuring timely processing of orders in accordance with cGMP. You will interface with QC, Operations, Logistics and QA to ensure compliant handling of samples and documentation

Start Date: 01/10/2025

Place of Work: Visp

Key Responsibilities

  • Checking and transferring reserve, shipping, and stability samples
  • Checking retention samples
  • Issuing reserve and stability samples
  • Storing retention samples
  • Compliance with quality (SOP and GMP) and safety regulations
  • Interfaces with QC project manager, QC shift, operations, logistics, and QA

 

Candidate Profile

  • 1-3 years of relevant experience
  • Strong organizational and communication skills
  • Proficiency in English required, German is a big plus

Job ID 41181183