CEO NECST
Wat ga je doen?
The mission of NecstGen is to translate the results of research performed at LUMC, other academia and pharmaceutical industry into clinical programs and actual patient treatments by means of product development and pharmaceutical manufacturing in a GMP environment, leading to patients being served with ground breaking cell and gene therapy in a reliable and predictable manner.
In short
- As CEO you are ultimately responsible for the GMP facility NecstGen
- You report to the LUMC board of directors. LUMC is 100% shareholder
- The facility has been built and is operational with all appropriate GMP licenses in place
- A team of international top-talented employees and management functions are in place
- The facility is in its scale-up phase, working on existing contracts with clients and onboarding new clients while the first tech transfer and manufacturing has started
- Proven capability of reliable process/product development & manufacturing of cell and gene products are a top priority: to serve customers and their patients, and to build up a solid company reputation with both customers and regulatory authorities
- Robust quality management and GMP compliance is the license to operate and thus a critical success factor
- Revenue growth through additional CDMO contracts with key clients is also a key priority and the outcome of the above. We are aiming at a balanced mixture of commercial and academic manufacturing
What you will do
- Position NecstGen in the market as the CDMO of choice for cell and gene product development and GMP manufacturing
- Growing the business, capitalizing on commercial opportunities working closely with pharmaceutical clients
- Working closely with academia, develop strong relations with key academic players leading to a sustainable portfolio of academic projects
- Developing the organization for the next phase from start up to running business with a sustainable P/L
Waar ga je werken?
NecstGen is a leading CDMO (Contract Development and Manufacturing Organization) focused on process development and GMP manufacturing of cell and gene therapies. We are an independent, non-profit organization with a state-of-the-art facility in Leiden, specifically designed to develop, manufacture, and deliver these complex therapies to patients.
NecstGen is an independent subsidiary of the Leiden University Medical Center (LUMC). Thanks to this independent position, we can fully focus on innovation and accessibility in cell and gene therapy. Our location at the Leiden Bio Science Park, one of Europe’s largest life sciences clusters, offers direct access to a network of experts, partners, and emerging talent.
By investing in advanced manufacturing technologies and strategic collaborations, we support academic institutions, start-ups, and biopharmaceutical companies in scaling up their innovative therapies. Our expertise and flexible approach enable organizations to execute complex manufacturing processes efficiently and according to the highest quality standards.
Wat neem je mee?
- 10 years + experience in the field of GMP pharma/ bio-tech industry
- Proven track record in pharmaceutical business development, product development, quality management and manufacturing
- Familiar with developments in cellular and gene therapy
- Strong communication skills and excellent networker
- Experience in growing and structuring a mid-size business
- Proven track record in leadership
Wat bieden we jou?
- Contributing to the future of healthcare with innovative cell and gene therapies
- Working in a modern, high-tech environment with the latest equipment
- Being part of a close-knit and motivated team where collaboration and growth are central
- The opportunity for professional development in a fast-growing sector with many career advancement opportunities
- Working at a strategic location in the Leiden Bio Science