In this role, you act as the QC representative within cross-functional project teams, serving as the main interface to internal and external stakeholders. You ensure alignment between quality control, production, and quality functions while driving efficient project execution. The position requires strong coordination skills, sound GMP knowledge, and the ability to manage priorities in a dynamic environment.

Start Date: 02/02/2026

Duration: 11 Months

Place of Work: Visp

Key Responsibilities

  • Establish and maintain strong relationships with internal and external customers
  • Represent QC as the single point of contact within cross-functional project teams
  • Plan, prepare, and oversee production campaigns from a QC perspective
  • Manage change requests and deviations in compliance with GMP requirements
  • Coordinate and support customer audits and regulatory inspections
  • Plan, track, and control QC-related project costs
  • Independently prioritize, coordinate, and schedule QC activities across laboratories

Candidate Profile 

  • Master’s degree or PhD in a natural science such as biology, biochemistry, or pharmaceutical sciences
  • Professional experience in a GMP-regulated environment, ideally within quality control
  • Fluent communication skills in both German and English
  • Confident user of standard office software such as MS Office
  • Familiarity with pharmaceutical or laboratory systems such as LIMS, Trackwise, or Documentum is an advantage
  • Strong organizational skills with the ability to manage complex tasks and shifting priorities
  • Structured, proactive, and solution-oriented working style with a collaborative mindset

Job ID 18507