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Join a forward-thinking company in the Cell & Gene Therapy sector as a Tech Transfer Specialist. This exciting role involves managing the transfer of scalable manufacturing processes into a state-of-the-art facility, contributing to the advancement of cutting-edge therapies. You will collaborate with various teams to ensure timely delivery of project goals while maintaining quality standards. If you have a passion for innovation and a strong background in GMP manufacturing and process development, this opportunity is perfect for you to make a meaningful impact in the field.
Job Description: This is an exciting opportunity to join a leading company in the Cell & Gene Therapy sector. We are seeking a skilled Tech Transfer Specialist to manage the transfer of scalable manufacturing processes, projects, and knowledge into a state-of-the-art facility. This role offers the chance to play a key role in advancing cutting-edge therapies, including commercial-scale production and government-funded projects.
Purpose of the Role: The Tech Transfer Specialist will oversee the successful transfer of manufacturing processes, projects, and knowledge into a new, high-tech manufacturing site. You will collaborate with internal teams to ensure that all technical processes and projects meet timelines and quality standards.
Key Responsibilities:
Manage the end-to-end transfer of internal and external tech transfer activities, including outsourced process development and GMP manufacturing processes.
Collaborate with the Innovation Team and Process Development groups to manage the transfer of scalable manufacturing processes.
Ensure timely delivery of project goals, working with external Contract Manufacturing Organizations (CMOs) in technical collaboration.
Oversee the transfer of processes both into and out of the manufacturing facility.
Maintain the site-wide Quality Management System (QMS).
Contribute to the design, development, and implementation of key projects at the facility.
Desired Skills and Experience: To succeed in this role, candidates should have:
Demonstrable experience in GMP manufacturing of ATMPs, biologics, or related sectors.
Strong understanding of both upstream and downstream processing.
Experience with cell culture of human or mammalian cell lines.
Experience in the writing of Batch Records or manufacturing protocols.
A BSc or higher qualification in a relevant life science field.