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September 18, 2026

Project Manager

Mid • On-site

Trofa, Portugal

Quick Facts

  • Role: Project Manager (Mid to Senior)
  • Focus: Cross-functional, end-to-end delivery of complex projects
  • Domain: Life Sciences valued

Description

Lead the end-to-end delivery of complex projects, ensuring scope, quality, budget, and timelines are consistently met. You will act as the primary liaison between technical teams, business stakeholders, and client partners, defining scope, milestones, deliverables, resources, and dependencies. You will manage risks, champion governance and project methodologies (Agile, Hybrid, Waterfall), and provide regular reporting to senior management and steering committees.

Responsibilities

  • Deliver complex projects end-to-end while meeting scope, quality, budget, and timeline targets
  • Serve as liaison between technical teams, business stakeholders, and client partners
  • Define project scope, milestones, deliverables, resources, and dependencies
  • Perform risk assessment, mitigation tracking, and remove project bottlenecks
  • Implement and champion established governance and project methodologies (Agile, Hybrid, Waterfall)
  • Provide regular status reporting, dashboards, and presentations to senior management and steering committees
  • Foster collaboration within cross-functional project teams

Requirements

  • 4 to 8+ years of project management experience (consulting, enterprise technology, or regulated domains preferred)
  • Mid-level to Senior profile
  • Full professional proficiency in English (minimum C1) with excellent communication and stakeholder management
  • PMP, PRINCE2, AgilePM, or equivalent certifications strongly preferred
  • Strong knowledge of Agile frameworks (Scrum/Kanban) and/or traditional project lifecycles
  • Ability to define scope, milestones, deliverables, resources, and dependencies
  • Ability to manage risk assessment and mitigation tracking effectively

Benefits

Not specified in the provided posting.

Valued Assets (Nice to Have)

  • Life Sciences background (Pharmaceuticals, Biotech, Clinical Operations, Medical Devices) or academic background
  • Familiarity with strict regulatory compliance and validation frameworks

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