Project Manager (m/f/d)

General Information:

- Start date: 03.02.2025

- End date: 31.12.2025

-Location: Visp, Wallis

Key Responsibilities:

• Act as the primary accountability point for project integration, aligning EPCM and production activities.
• Develop and manage comprehensive project plans, including timelines, deliverables, and milestones.
• Lead cross-functional coordination among engineering, production, QA, and validation teams.
• Oversee GMP change control processes (e.g., TCRs, CRs) and ensure compliance with regulatory standards.
• Collaborate with the Engineering Project Manager to monitor EPCM contractor performance.
• Plan and execute validation activities, including performance qualification (PQ).
• Provide regular updates to senior management, highlighting risks and mitigation strategies.

Qualifications:

• Education: Bachelor’s degree in Engineering, Biotechnology, or related field (Master’s preferred).
• Experience: 6–8 years of project management in CapEx/GMP-regulated environments, preferably biopharma.
• Skills: Proficiency in project management tools (MS Project, Primavera); strong understanding of GMP principles and change management.
• Certifications: PMP or PRINCE2 preferred; Lean Six Sigma a plus.