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.
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