Project Manager CAPEX

03 November 2021
SalaryNegotiable
LocationHoofddorp
Temporary
DisciplineLife Science CareersProject/Program Management
ReferenceBBBH492060_1635953981

For our client, a Biotechnology company in Hoofddorp, we are looking for a Project Manager CAPEX.

Role

The new Project Manager CAPEX will deliver 'best in class' projects that meets strict safety, quality, capital and schedule requirements, leading and executing from definition to handover for both small and medium size biopharmaceutical critical capital projects linked to the manufacturing site strategy.

Your responsibilities will be to:

  • Lead and provide guidance for the design, planning and execution of the entire project lifecycle for equipment, facilities and utilities CapEx projects
  • Develop and implement project plans. Own project execution and guide a multidisciplinary team from inception through project completion
  • Manage activities leading to the successful execution of assigned projects
  • Collaborate with cross-functional teams, equipment design vendors, architects, engineers, project sponsors, other departments, and external stakeholders to prepare business cases and justify capital for new projects
  • Communicate across functional and leadership teams to inform project status and risks, elevate issues, present recommendations, and implement modifications or project plans
  • Ensure compatibility and consistency with existing organization and industry standards
  • Leadongoing project risk analysis as well as mitigation plan and leadcontinuanceimprovementprocessthroughlesson & learnedsessions
  • Create and deliver project presentations to cross-functional stakeholders to ensure that phase transitions are efficient and comprehensive
  • Manage and build relationships with equipment suppliers and external engineering consultants


Requirements

  • MSc/BSc Degree in Engineering or Technology
  • 5+ years of CapEx Project Management experience (Pharma/Biotech/Medical Device/Chemical/Food/Semiconductor) - CAPM, PMP or PRINCE II preferred
  • Project Management knowledge of tools, techniques, culture, software applications (Microsoft Project)
  • Knowledgeable with cGMP manufacturing as well as regulatory regulations and requirements for pharmaceutical products and drug development process
  • Knowledge of the GAMP validation model and ASTM E2500; familiarity with equipment specifications and validation lifecycle (FAT, SAT, IQ, OQ, PQ)
  • Great interpersonal communication and team building skills - ability to lead cross functional teams
  • High emotional intelligence, with demonstrated ability to successfully negotiate through challenging situations and difficult conversations.


What do we offer

  • 6 month contract at a company working towards eliminating the burden of chronic cancer care.
  • Start date: ASAP
  • An international, dynamic and fast-paced environment where discoveries are made every day.


Marcella Henryati
T: +31 6 588 11 958
When interested please react through the application process with your English resume.

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