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Acino

Project Manager

Acino Egypt

Pharmaceutical Manufacturing · 1,001-5,000 employees

Jun 24
project-manager Senior (5-10 yrs) Full-time Egypt
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About the role

The project manager will lead the full project lifecycle within a pharmaceutical manufacturing environment, ensuring all activities align with GMP, safety, quality, and budget requirements. They will coordinate cross-functional teams and manage stakeholders to drive project success from initiation to closure.

What they look for

Project management Pharmaceutical manufacturing GMP compliance Regulatory compliance Cross-functional team coordination Budget management CAPEX Risk assessment Project lifecycle management Project planning Scheduling Vendor management Stakeholder management KPI monitoring Leadership Problem-solving

Requirements

Candidates must have at least 7 years of experience in project management, preferably within the pharmaceutical or a regulated industry. A proven track record in managing cross-functional projects, budget control, and regulatory compliance is essential for this role.

Full description

Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide.

The job holder will manage and deliver projects within a pharmaceutical manufacturing environment, ensuring execution aligned with GMP, safety, quality, timeline, and budget requirements while supporting business objectives. the position will be engaged across all site levels and should have hand on experience with project management expertise, the job holder will report to Egypt Site Head and located in our site in Al Obour City. 

Key Responsibilities:

  • Lead full project lifecycle from initiation to closure
  • Define scope, deliverables, timelines, and resource needs
  • Develop and maintain project plans
  • Coordinate cross-functional teams (Production, QA, Engineering, Supply Chain, EHS)
  • Ensure compliance with GMP and regulatory requirements
  • Monitor project progress, risks, and KPIs
  • Manage project budgets and CAPEX spending
  • Drive risk assessment and mitigation plans
  • Provide regular reporting to stakeholders
  • Manage contractors and vendors where applicable

Qualifications & Experience:

  • 7+ years' experience in project management
  • Experience in pharmaceutical manufacturing or regulated industry
  • Proven track record managing cross-functional projects
  • Project lifecycle management
  • Project planning & scheduling
  • Budget (CAPEX) and cost control
  • Risk assessment & mitigation
  • GMP & regulatory compliance
  • Cross-functional team coordination
  • Stakeholder & vendor management
  • KPI monitoring & performance tracking
  • Problem-solving & decision-making
  • Strong communication & leadership skills

This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!

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