Job Description

Job Responsibilities:

• Lead and manage CAPEX and tech transfer projects in a cGMP manufacturing environment.
• Drive full project lifecycle: planning, execution, monitoring, control, and closure.
• Develop and manage project plans, timelines, budgets, and risk mitigation strategies.
• Coordinate and lead cross-functional teams including engineering, operations, quality, and external vendors.
• Oversee design, construction, commissioning, and change control activities.
• Ensure projects meet cost targets, timelines, and quality standards.
• Communicate project status, risks, and financial updates to senior leadership.
• Manage vendor sourcing, contracting, and performance (design, construction, equipment providers).
• Ensure compliance with cGMP regulations and company governance processes.
• Identify and resolve complex project risks and issues independently.

Skills:

• 10+ years of project management experience, preferably in biopharma or manufacturing environments.
• Strong experience with CAPEX projects and tech transfer.
• Deep understanding of cGMP regulations and quality standards.
• MS Project
• Primavera
• Procore
• Bluebeam
• BIM tools

Education/Experience:

• Bachelors.

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