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