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Senior Quality Control Specialist, QC Project Lead

Job in 3930, Visp, Canton du Valais, Switzerland
Listing for: CTC Resourcing Solutions
Seasonal/Temporary position
Listed on 2026-01-04
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 80000 - 100000 CHF Yearly CHF 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Senior Quality Control Specialist, QC Project Lead - 6800
Location: Visp

Senior Quality Control Specialist, QC Project Lead (Job )

Contract Duration: ideally from 02.02.2026 to 31.12.2026 (possibility of extension). Workload: 100% (on-site, no home office).

Location:

Visp, Switzerland.

The Role:

As a member of the QC Project Lead team at the Visp site, you will be responsible for communication with production, QA and external customers. As a single point of contact in cross‑functional project teams, you will represent QC and drive strategic alignment in collaboration with QA, OPS, MSAT and engineering. The Project Leader is independent and makes decisions on QC representation.

Within the matrix organization of the project team, you will always be in close contact with the analytical laboratories as well as with the program management, process development, production, and quality assurance departments, among others. Through excellent planning and management of the project, you will ensure the timely and cost‑efficient processing of orders, even in the face of changing customer wishes and priorities.

Main Responsibilities:

  • Establishing and maintaining customer relationships
  • Preparation and supervision of production campaigns
  • Processing of change requests and deviations under GMP
  • Supervision of customer audits and inspections by authorities
  • Calculate and monitor QC costs in the project
  • Independent coordination, prioritization and scheduling of QC tasks

Qualifications and

Experience:

  • Master's or PhD in the natural sciences (biology, biochemistry or pharmaceuticals)
  • Experience in the GMP environment as well as in quality control is an advantage
  • Good communication skills in German and English are a must
  • Experienced handling of common software applications (MS Office) is required. Knowledge of individual pharmaceutical/laboratory software (e.g. Documentum, LIMS, Trackwise) is an advantage
  • Good comprehension and very good organizational skills round off your profile

Seniority level:
Mid‑Senior level

Employment type:

Contract

Job function:
Quality Assurance and Manufacturing

Industries:
Biotechnology Research and Pharmaceutical Manufacturing

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Position Requirements
10+ Years work experience
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