Biopharma Validation & Capital Projects Lead

Oxford Global Resources

Amsterdam

Vor Ort

EUR 73.000 - 78.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden
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Benefits dieser Stelle

12 month contract
Possibility to extend
Salary €6,500–€7,000 gross monthly
Amsterdam region

Zusammenfassung

Oxford Global Resources is seeking an experienced Engineering Project Manager to oversee capital engineering projects in a regulated biopharmaceutical manufacturing setting. You will drive the full project lifecycle from concept through implementation and transfer to operations, coordinating equipment, facilities and utilities with engineering specialists and operations teams.

You will manage schedules and risks, lead cross-functional groups, ensure adherence to cGMP and GAMP standards, and

Qualifikationen

  • 5+ years of project management experience in a cGMP environment.
  • Engineering background with BSc or MSc.
  • Familiarity with validation and qualification processes (GAMP).
  • Experience using PM tools and frameworks (PMP, CAPM, PRINCE2).
  • Experience with equipment lifecycle activities (FAT, SAT, IQ, OQ, PQ).

Aufgaben

  • Manage Capital Projects in a biopharmaceutical firm
  • Lead projects focused on manufacturing equipment, facilities, and utility lifecycles
  • Coordinate multidisciplinary teams to achieve project milestones and deliverables
  • Perform feasibility studies
  • Continuous risk analysis, mitigation and improvement
  • Create and present project updates to stakeholders and management

Kenntnisse

Project management
cGMP
Stakeholder coordination

Ausbildung

BSc or MSc in Engineering

Tools

PMP
CAPM
PRINCE2

Jobbeschreibung

Oxford Global Resources is seeking an experienced Engineering Project Manager to oversee capital engineering projects in a regulated biopharmaceutical manufacturing setting. You will drive the full project lifecycle from concept through implementation and transfer to operations, coordinating equipment, facilities and utilities with engineering specialists and operations teams.

You will manage schedules and risks, lead cross-functional groups, ensure adherence to cGMP and GAMP standards, and

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