Project Scheduler (m/f/d)

General Information:

• Start date: ASAP (03.02.2025)
• End date: 31.12.2025
• Location: Visp, Wallis

What You’ll Do:

• Develop and maintain comprehensive schedules, integrating EPCM and compliance activities
• Act as a central coordination hub across engineering, production, and quality teams
• Monitor project timelines, identify risks, and implement corrective actions
• Collaborate with QA/QC teams to align compliance activities with project milestones
• Leverage tools like Primavera P6 or MS Project to manage schedules effectively

What You’ll Bring:

• A Bachelor’s degree in Engineering, Life Sciences, or Project Management
• 3–5 years of scheduling experience in a regulated GMP environment, ideally in biopharma
• Expertise in project scheduling tools and GMP compliance processes
• Strong organizational skills and the ability to communicate effectively across teams