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Director Process and Analytical Development - Cell Therapy
Aussicht: 155
Update Tag: 26-11-2025
Kategorie: R & D IT - Software
Industrie: Biotechnology Research Pharmaceutical Manufacturing
Position: Director
Jobtyp: Full-time
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Jobinhalt
Location: Gosselies, BelgiumPosition Summary:The Director Process and Analytical Development - Cell Therapy is responsible for leading the P&AD team in the development, GMP translation, and technology transfer and associated analytical methods. The Director is expected to have a comprehensive understanding of Cell Therapy development paradigms for process and analytical development. Driving CMC activities and innovative solutions for early and late-stage client programs is critical for success. The Director is accountable for the operational activities of the P&AD platforms, including ensuring that people and project management process are in place and tracked.The Role:- Apply technical, functional, business, and/or industry knowledge to design experiments or project scopes; provide scientific or business consultation to the clients, business development, site and executive leadership team and manage multiple functions and/or focuses across site disciplines.
- Partner closely with prospective and existing clients, as well as Project Management and Business Development, to ensure client expectations, scheduling, and timelines are met.
- Work closely with the Project Management, Quality Control and Operations to ensure successful transfer of processes and analytics from P&AD and/or clients into manufacturing and validations in order to support early phase through commercial manufacturing activities.
- As a key technical leader for Catalent Cell Therapy; identify, assess and implement new process and analytical technologies to improve product yields, quality, success rate, reproducibility and/or reduce cost and time of manufacturing processes
- Serve as a key PD leader and build connections and collaboration across the Catalent network of Cell, Gene, Plasmid and Protein development teams.
- Lead a group of direct reports which may include principal level scientists; people leader reports are expected. Hire, mentor and develop a talented and diverse technical team. Lead team members to engage, improve and reinforce performance of others
- Manage strategic activities across departments and global sites. Define and lead multisite strategic initiatives.
- Other duties as assigned
- PhD in a relevant field, minimum 10 years in cell and gene therapy, pharma, or biotech managing a team as Senior Manager on site for at least 2 years or similar experience in a previous role.
- At least 10 years’ experience in ATMP/Cell and Gene Therapy/Vaccines CMC product development, including process and analytical method development.
- Experience in preparing regulatory submissions for CMC is a plus.
- Proficient in English verbal and written communication skills to convey and receive ideas and instructions from and to others within the organization.
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Frist: 10-01-2026
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