Senior Scientist (12 month fixed term), Global Technical Development at Orchard Therapeutics

London, England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

04 Jun, 26

Salary

0.0

Posted On

06 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process Development, Gene Therapy, HSC Manufacturing, Lentiviral Vectors, Regulatory Submissions, CMC Strategy, Data Analysis, Risk Assessment, Process Qualification, Tech Transfer, GMP Manufacture, Process Characterisation, Comparability Strategies, Risk-Based Analysis, CDMO Management, Experimental Design

Industry

Biotechnology

Description

Location: London, UK Reporting to: Senior Scientist, Global Technical Development Job Summary Orchard Therapeutics, a Kyowa Kirin company, is a global gene therapy leader focused on transforming the life of patients with rare disorders through innovative gene therapies based on gene-modified hematopoietic stem cell (HSC). Orchard has its global headquarters in London and U.S. headquarters in Boston. Technical Development sits within Technical Operations at Orchard and is responsible for the development and characterization of Lentiviral Vectors (LVVs) and Drug Substance/Drug Product production processes, which meet patient demand for therapeutic products of the best quality. The Senior Scientist, Global Technical Development will be primarily responsible to drive and support project activities for development of ex-vivo gene therapy manufacturing processes along the development pathway to the point of process qualification. The creation of high-quality source documents and expert review of regulatory documents to support IND/CTA and BLA/MAA filings is a key component of this role. They would be heavily involved with both the Process Development Team and CMC Program team, working on cell process development and collaborating with other functions to drive key project goals. Key Elements and Responsibilities · Design manufacturing processes and characterize gene modified HSC processes and products to deliver robust platforms for early and late-stage clinical development. · Design complex experiments, perform data analysis and author reports suitable for regulatory submissions using senior-level judgement and expertise. · Provide expert compilation of documents. This includes risk assessments, development protocols and reports, batch records, standard operating procedures and investigations. · Preparation CMC regulatory submissions (e.g. INDs, BLAs, Scientific advice) and source documents. · Provide strategic input into development plans, program CMC strategies and departmental/functional activities, and deliver on agreed actions. · Present development strategy plans and results to the wider department and functional teams, and discuss conclusions and next steps. · Co-ordinate development activities with preclinical, QA and other departments to ensure the achievement of company timelines and milestones. · Lead oversight of development at company designated Contract Development and Manufacturing Organizations (CDMOs). · Collaboratively participate in multi-disciplinary teams to perform risk-based analysis of processes where appropriate and providing impact assessments as required. · Identify and implement validation requirements pre PPQ, in accordance with current industry and CMC regulatory standards and best practices in of cell and gene therapy. · Other activities may be assigned. Required Knowledge & Experience As a proven technical scientific expert in the development, manufacture and delivery of cell-based therapy products with significant applied experience in the biotechnology industry, this candidate will possess: · Substantial experience in the biotechnology or pharma industry e.g. PhD+ >4 years’ experience (depending on scope and relevance), with a primary focus on the development, manufacture, and delivery of cell and gene therapy products · In-depth technical experience with a proven track record of developing, integrating and implementing equipment and processes for clinical and/or commercial application. · Understanding of Tech transfer and GMP manufacture · In-depth knowledge of process development, process characterisation and comparability strategies · Experience with risk-based approaches, such as Failure Modes and Effects Analysis · Experience and understanding of Process Validation, ideally in cell and gene therapy · Gene therapy specific regulatory understanding and experience preferred · Experience with and authoring regulatory filings and associated reports/sections writing. · DOE and QBD experience a plus · Experience of external CDMO management and building strong external relationships Skills and Abilities · Excellent interpersonal skills and demonstrated ability to work in a matrix environment · Excellent written and oral communication skills, including presenting to senior management/executives · Outstanding organizational skills · Creative problem solver · Ability to operate in a fast-paced, multi-disciplinary industrial environment · Collaborative Communication – works effectively across diverse teams and external partners; communicates clearly and persuasively. · Adaptability – thrives in dynamic, fast-paced environments with shifting priorities. · Critical Judgment – makes sound decisions based on data, risk, and strategic goals. Education · BSc, MSc or PhD or equivalent, in bioprocessing, biological sciences, gene therapy or related subject

Responsibilities

The Senior Scientist will primarily drive and support project activities for developing ex-vivo gene therapy manufacturing processes up to process qualification, focusing heavily on creating high-quality source documents and reviewing regulatory documents for filings. They will collaborate with the Process Development Team and CMC Program team on cell process development to achieve key project goals.