Visp
24 months
40 hours
SL-000923
SL-000923
Job description
Start: 01.05.2026
Duration: Until 01.04.2027
Workload: 100%
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
