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Senior Process Development Scientist - Cell Therapy

Job LocationLondon
EducationNot Mentioned
Salary40,000 - 44,000 per annum
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent , full-time

Job Description

We have an exciting opportunity for a Senior Process Development Scientist to join a UCL supported cell therapy program. You will play a key role in the manufacturing of cells under GMP conditions for use in a clinical trial, ultimately to help develop acell product for use in a glaucoma therapy. You must be educated to BSc level in a biology subject and have experience of working in process development, in particular, developing protocols around the translation of ATMP / cell therapy products. This is a 12 month contract.Duties and responsibilities

  • Aseptic Stem cell culture and preparation of retinal organoids under GMP conditions.
  • Aseptic preparation of tissue culture media, supplements and reagents.
  • Independently manage the process development / translation of research protocols into a GMP-compliant process
  • Routine maintenance of the clean room environment and ancillary facilities, including equipment checks and calibration, ordering, environmental monitoring and cleaning.
  • Ensuring that good working practice in the laboratory is upheld and that all Health & Safety procedures relating to the work is comprehensive and up to date.
  • To manage interactions with commercial suppliers and service technicians.
  • To ensure targets are achieved.
  • To present and collate data for presentations.
  • To write and update Standard Operational Procedures and Risk Assessments as required.
  • RNA isolation
  • FACS analysis
  • Process data using software such as Matlab
  • Work collaboratively with other members of the team
  • The postholder will actively follow UCL policies including Equal Opportunities and Race Equality policies
Experience Required:
  • Minimum requirement is a BSc or MSc degree in a biological science.
  • Experience of working in compliance with Good Manufacturing Practice as it applies to ATMP / cell therapy production
  • Experience of working in process development, in particular, developing protocols around the translation of ATMP / cell therapy products
  • Proven competence working in a Grade B cleanroom, including media and supplement preparation, cell culture, cleaning and environmental monitoring
  • Knowledge and understanding of the ATMP and EUTCD Directives
  • Ability to complete documentation in accordance with MHRA regulations for cell therapy production

Keyskills :
Cell Therapy - Stem Cell - ATMP - Ophthalmology - GMP

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