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  • Location: Cambridge
  • Salary: Competitive Salary
  • Job Type:Permanent

Posted 12 days ago

  • Sector: Scientific Development
  • Contact: Georgie Lamberth
  • Contact Email: georgie.lamberth@nextphaserecruitment.com
  • Contact Phone: 014032 16216
  • Start Date: ASAP

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.