Supply Chain Quality Specialist

• Life Sciences - Supply Chain / Operations
• Wallis
• Contracting
• Vollzeit
• 01.09.2026 - 31.12.2026 (with the chance of extension)
• Supply Chain

Start Date: 01.09.2026
End Date: 31.12.2026 (with the chance of extension)
Workload: 100% with 41h/week
Location: Visp
Workmodel: Contracting

Your responsibilies

• Coordinate and support the end-to-end management of GMP-related Change Requests and Concept Changes in TrackWise.
• Ensure changes are appropriately assessed, documented, reviewed, approved, implemented, and closed according to applicable GMP and QMS requirements.
• Partner with Supply Chain, Quality Assurance, Manufacturing, Engineering, IT, and other stakeholders to complete impact assessments, risk assessments, and implementation planning.
• Monitor progress of open change activities, proactively follow up on actions, and support timely closure of records.
• Develop, document, and maintain standardized procedures, operating standards, and work instructions for recurring Supply Chain change management activities.
• Capture lessons learned and best practices while managing different types of Change Requests and Concept Changes, translating them into clear and sustainable ways of working.
• Support governance activities, reporting, and metrics related to change management and supply chain quality processes.
• Provide guidance to stakeholders on TrackWise workflows, documentation expectations, and approved ways of working.
• Identify opportunities to simplify, harmonize, and continuously improve quality-related Supply Chain processes.
• Support audit and inspection readiness activities related to change management, documentation, and quality systems. 

Your Profil:

• Experience managing Change Requests, Concept Changes, Change Controls, Deviations, CAPAs, or related GMP quality processes
• Hands-on TrackWise software experience is highly valuated
• Good understanding of Quality Management Systems, GMP requirements, and documentation standards
• Experience developing or maintaining procedures, work instructions, standards, or business process documentation
• Quality Assurance or Quality Systems background is highly valued
• Strong stakeholder management, facilitation, and cross-functional collaboration skills
• Ability to work independently in a remote setup and drive activities with limited supervision
• Strong organizational, analytical, follow-up, and communication skills