Making Project Management Matter: Rethinking Delivery, Transformation, and Innovation in Life Sciences
Date: 19 November 2026 | 10:00–19:00
Location: PlusUltra, Emmy Noetherweg 2, 2333 BK, Leiden, the Netherlands
On 19 November 2026, the ISPE Benelux Project Management Community of Practice invites you to an exiting seminar Making Project Management Matter: Rethinking Delivery, Transformation, and Innovation in Life Sciences, where we will examine the evolving role of project management in supporting successful outcomes across the pharmaceutical and biotechnology sectors. Join project professionals, industry leaders and innovators from across the life sciences sector for a day of inspiring discussions, fresh perspectives and meaningful networking.
We look forward to welcoming you to a day dedicated to shaping the future of project management in life sciences!
Event Properties
| Event Date | 19-Nov-2026 10:00 - 19:00 |
| Capacity | 100 |
| Registered | 2 |
| Individual Price | 95 EUR. For ISPE members: 75 EUR |
| Location | Plus Ultra Leiden |
Agendas
| 10:00 |
Arrival & Registration |
| 10:30 |
Opening & Introduction ISPE PMCoP |
| 10:45 |
Martyn Smith"A roadmap to GMP Digitalization" |
| 12:15 |
Lunch & Networking |
| 13:15 |
Christopher Dohm"What Really Makes a Project Successful? Lessons learned from more than 30 years of project management, beyond time, cost and scope" |
| 14:00 |
Marloes Dijkhuizen"Leading Through Dual Transformation: Delivering a Portfolio-Wide MDD (Medical Device Directive) to MDR (Medical Device Regulation) Labeling Transition During Post-Merger Integration" |
| 14:45 |
Coffee break |
| 15:00 |
Final session: TBD |
| 16:00 |
Panel Discussion and Q&A |
| 16:30 |
Closure |
| 16:40 |
Networking & Drinks |
Speakers
Martyn Smith
Global Head of CSV/DI at Centrient Pharmaceuticals
Martyn Smith is Global Head of CSV/DI focusing on GMP-AI/GMP-Digitalisation and has more than 25 years of experience in pharmaceutical quality, computerised systems and validation. Throughout his career, Martyn has held senior QA, CSV and data integrity roles at companies including Centrient Pharmaceuticals, Janssen, GSK, Pfizer and Eli Lilly. His experience spans computer system validation, data integrity, digitalisation and the implementation and oversight of GxP computerised systems in regulated pharmaceutical environments. In his presentation, “Roadmap to GMP Digitalisation,” Martyn will explore the journey towards digitalisation in a GMP-regulated environment, drawing on his extensive experience in pharmaceutical quality and computerised systems. He will discuss how organisations can approach GMP digitalisation while maintaining regulatory compliance and managing the challenges associated with introducing new digital technologies.
Marloes Dijkhuizen
Managing Consultant at Progress
Marloes Dijkhuizen is a Managing Consultant at Progress with extensive experience in the biopharmaceutical industry. She is an accomplished CMC and manufacturing leader who has successfully led numerous development and commercialization projects across the product lifecycle, from early-stage development through commercial manufacturing. Throughout her career, Marloes has held a variety of international leadership roles spanning clinical and commercial manufacturing, CMC technology transfer, CDMO management, project management, and operational leadership. She brings deep expertise in large molecule drug substance development and manufacturing, process validation, strategic partnerships, and organizational transformation. As a consultant, Marloes supports biopharmaceutical companies in navigating complex manufacturing and supply challenges, driving operational excellence, and enabling successful product development and commercialization. She holds a Master of Science in Biomedical Sciences.
