Location: Visp (on-site, no home office)
Requirements
* Lead technical expansion and capacity-increase projects within Drug Product manufacturing to support production ramp-up
* Provide technical and operational input to project design, ensuring compliance with GMP and regulatory standards, including EU GMP Annex 1
* Coordinate cross-functional teams and external suppliers, supporting project governance and ensuring delivery within scope, budget and timelines
* Develop and implement best-practice processes aligned with current industry expectations and regulatory trends
* Manage project-related change controls, troubleshooting and deviations, including equipment-related investigations
* Establish and update operational procedures in close collaboration with manufacturing and quality teams
Competences
* Minimum 2 years of technical experience in GMP manufacturing (Drug Product preferred)
* Proven experience in project coordination or project management within pharmaceutical operations
* CAPEX project exposure and equipment qualification experience are strong advantages
* Solid understanding of cGMP and Annex 1 requirements
* Fluent in English; German is an advantage
* Strong collaboration skills, proactive mindset and ability to deliver under pressure with changing priorities
Maybe not for you, but for someone else?
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