Requirements: English
Company: i-Pharm Consulting
Region: north holland, north holland, the netherlands , 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