Added: 2025-05-28 14:10.00
Updated: 2025-05-30 03:32.41

Engineering Project Manager

North Holland, Netherlands

Type: n/a

Category: Engineering & Manufacturing

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Requirements: English
Company: i-Pharm Consulting
Region: North Holland

Are you passionate about leading impactful technical projects in a cutting-edge biopharma environment? Do you thrive in fast-paced, high-stakes settings where precision, innovation, and collaboration are key? Ready to take ownership of capital projects that directly support the future of life-changing therapies? If so, this could be the next exciting step in your career. We are looking for a highly organized, proactive, and detail-oriented Engineering Project Manager to join our advanced manufacturing site in Amsterdam. In this role, youll lead small to medium-scale capital projectsfrom concept through to completionensuring exceptional delivery across safety, quality, budget, and timeline metrics. Key Responsibilities Lead the full lifecycle of capital investment projects involving equipment, facilities, and utilities. Conduct feasibility studies and develop clear, technically sound project proposals. Develop and manage detailed project plans while guiding multidisciplinary teams. Oversee construction and technical execution in compliance with safety and quality standards. Collaborate with cross-functional teams and external partners to justify capital investments and align with strategic goals. Communicate project updates, risks, and solutions to leadership and stakeholders. Ensure consistency with internal standards and regulatory requirements. Drive continuous improvement through risk analysis and post-project lessons learned. Present project progress and outcomes to cross-functional stakeholders. What You Bring BSc or MSc in Engineering, Technology, or a related field. 5+ years of experience in technical project management within Pharma, Biotech, Medical Devices, Chemicals, Food, or Semiconductors. CAPM, PMP, or PRINCE2 certification preferred. Strong command of project management tools and methodologies; experience with Microsoft Project. In-depth understanding of cGMP manufacturing and relevant regulations. Familiarity with GAMP, ASTM E2500, and validation processes (FAT, SAT, IQ, OQ, PQ). Excellent leadership, interpersonal, and communication skills with a collaborative mindset. High emotional intelligence and a strategic approach to problem-solving. Why Join Us? Be part of a mission-driven organization thats reshaping the future of biopharmaceutical innovation. In this role, your work will directly support the production of therapies that change lives. Join a dynamic, collaborative team where your expertise is valued, and your impact is tangible. Apply now to discuss the opportunity in further detail
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