Pharmaceutical Capital Projects Manager | GMP & C&Q Expert

Legal Project Management Partners; Arecibo (PR); Presencial; USD 90 000 - 130 000; Tempo integral

Resumo da oferta

Legal Project Management Partners in ARECIBO, PR, is seeking a Project Manager to lead capital projects across automation, utilities, and infrastructure. You will drive planning, budgeting, and scheduling while coordinating Engineering, Validation, Quality, Manufacturing, Facilities, and external vendors to ensure on-time project delivery within GMP guidelines.

The role requires strong leadership, communications, and organizational skills, managing multiple projects in a regulated pharmaceutical

Qualificações

• Bachelor's degree in a technical field (Engineering, Life Sciences, or related)
• PMP or similar certification is a plus

Responsabilidades

• Lead and manage capital, automation, utilities, infrastructure, and C&Q projects from planning through completion.
• Develop schedules, timelines, budgets, and resource plans.
• Coordinate cross-functional teams across Engineering, Automation, Validation, Quality, Manufacturing, Facilities, Utilities, Construction, and external vendors.
• Monitor progress and ensure milestones are met.
• Ensure GMP, FDA, and regulatory compliance.
• Support commissioning, qualification, validation, and startup activities.
• Maintain project documentation and records.
• Provide status updates to stakeholders and leadership.

Conhecimentos

Project management

Leadership

Communication

Regulatory compliance

GMP/FDA knowledge

Cross-functional collaboration

Stakeholder management

Problem solving

Formação académica

Bachelor's degree in Engineering/Life Sciences/Pharmaceutical Sciences

PMP Certification (or similar)

Ferramentas

Microsoft Office Suite

Project management tools

Descrição da oferta de emprego

Legal Project Management Partners in ARECIBO, PR, is seeking a Project Manager to lead capital projects across automation, utilities, and infrastructure. You will drive planning, budgeting, and scheduling while coordinating Engineering, Validation, Quality, Manufacturing, Facilities, and external vendors to ensure on-time project delivery within GMP guidelines.

The role requires strong leadership, communications, and organizational skills, managing multiple projects in a regulated pharmaceutical