Orchard Therapeutics is hiring a

CMO Support Associate EU

London, United Kingdom

Orchard Therapeutics is a fully integrated commercial-stage biopharmaceutical company dedicated to transforming the lives of patients with serious and life-threatening rare disease through innovative gene therapies.


Orchard’s portfolio of autologous ex vivo gene therapies includes Strimvelis, the first autologous ex vivo gene therapy approved by the European Medicines Agency for adenosine deaminase severe combined immunodeficiency (ADA-SCID). Additional programs for neurometabolic disorders, primary immune deficiencies and hemoglobinopathies include three advanced registrational studies for metachromatic leukodystrophy (MLD), ADA-SCID and Wiskott-Aldrich syndrome (WAS), clinical programs for X-linked chronic granulomatous disease (X-CGD) and transfusion-dependent beta-thalassemia (TDBT), as well as an extensive preclinical pipeline.


Reporting to: Senior Manager EU, Cell Therapy Operations


The CMO Support Associate will support activities related to the manufacture of Orchard Therapeutics’ innovative gene-modified cell-based therapeutic products. Such activities will include becoming a subject matter expert on the manufacturing process and communicating closely with personnel at contract manufacturing organizations to track and manage activities. This role is ideal for someone looking to work in a small team, where a person’s contribution is valued.


RESPONSIBILITIES


  • Become a subject matter expert on the full manufacturing process, including the isolation, culture, transduction, and cryopreservation of cells, as well as drug product shipping processes
  • Train manufacturing operators
  • Support implementation of process changes
  • Track and trend manufacturing run data
  • Track manufacturing raw material inventory and order materials
  • Provide person-in-plant support for manufacturing runs
  • Contribute to the compilation and review of master production records, standard operating procedures, development/validation protocols, and reports
  • Contribute to the review of executed batch records
  • Support investigations of deviations and non-conformances
  • Participate in cross-functional activities with Process Development, Process Validation, Quality Assurance, Quality Control, Analytical Operations, Clinical Development, and commercial departments to ensure the successful achievement of company timelines and milestones
  • Provide data summaries for CMC / CTD documents for regulatory filings with US and EU regulatory agencies
  • Other activities as may be assigned

Requirements

The ideal candidate for this position must have experience in the manufacture and delivery of cell-based therapy products with significant applied experience in the biotechnology industry.


Candidate must possess:

  • A BS or equivalent in bioprocessing, medical technology, chemical engineering, or biological sciences
  • Experience in the biotechnology or pharma industry with a primary focus on the development, manufacture, distribution and delivery of cell-based therapy products
  • Experience with technology transfer of manufacturing processes and controls at CMOs
  • Familiarity with FDA, EMA, GMP and ICH regulatory requirements is advantageous
  • Excellent organizational skills
  • Excellent written and oral communication skills
  • Ability to operate in a fast-paced, multi-disciplinary industrial environment
  • This position requires on site person-in-plant presence at CMOs and contract vendors on a potential global basis. Therefore, ability to travel is a prerequisite.

Benefits

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