Career Opportunities in the Foresite Capital Network

Location: London, UK

Reporting to: Principal Scientist, Cell and Gene Technical Development

Job Summary:This is an exciting opportunity for a well-qualified candidate to join an international company focused on transforming the lives of patients with rare disorders through innovative gene therapies.

Orchard Therapeutics, Ltd. (OTL) is looking for a Scientist I or II (depending on experience) for the Process Development team, focused on the development of analytical assays for Orchard Therapeutics innovative gene-modified cell-based therapeutic products. Primary activities will include developing, validating and performing analytical assays for process development, QC and characterization of lentiviral vector and HSC gene therapy products. The post may also include research with internal departments and external partners, including development, validation and technology transfer, to support OTL’s product pipeline programs.

The role will be based in Orchard’s London Hammersmith site where the state-of-the-art development laboratories are located.

Key Elements and Responsibilities

1. Develop, validate and perform analytical assays for process development, implementation as QC and/or characterization assays for lentiviral vector and HSC gene therapy products

2. Involvement in the transfer of processes and analytical methods from external collaborators and internal Orchard Research team to the Technical Development team.

3. Assessment of novel equipment and methodologies for lentiviral vector and HSC DP analytics.

4. Participate in the Technical Development team through generation and testing of lentiviral vectors, and involvement in the optimization and improving lentiviral vector and HSC manufacturing processes.

5. Assist in lab management duties, stock management and equipment maintenance and other practical day-to-day activities in the lab.

6. Keep accurate and contemporaneous records of all development activities and analysis in Orchard’s electronic lab notebook, presentations and/or reports, and present to the wider team/department.

7. Authoring, reviewing and editing batch records, SOPs, development protocols and reports for internal and external analytical development, and CMC regulatory submissions.

8. As required, manage activities at CDMOs and CTOs for the tech transfer, development, and validation of analytical methods, including the design, review and approval of associated protocols, test records/forms, reports and SOPs.

9. Other activities may be assigned as required, in agreement with line management.