At a Glance
- Tasks: Lead the development of innovative processes for viral vector production.
- Company: Join Orchard Therapeutics, a global leader in gene therapy based in London.
- Benefits: Enjoy a dynamic work environment with opportunities for personal and professional growth.
- Why this job: Be part of a mission to transform lives through cutting-edge gene therapies.
- Qualifications: PhD or equivalent in relevant scientific fields; 5+ years in viral vector development required.
- Other info: Collaborate with diverse teams and contribute to groundbreaking therapeutic advancements.
The predicted salary is between 54000 - 84000 £ per year.
Location : London (Hammersmith) Reporting to : Director, Viral Vector Development 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 DS/DP production processes, which meet patient demand for therapeutic products of the best quality. Reporting to the Director, Viral Vector Development, the Principal Scientist, Viral Vector Development, will be responsible for the development of innovative, high-yield processes for production of LVVs. The candidate will closely interact with other functional groups including analytics, cell process development, CMC and regulatory teams. This role is based in our Hammersmith, London facilities within our global headquarters and will suit candidates who would like to join a global company with a diverse and dynamic work environment that provides opportunities for sustained personal and professional growth. Key Elements and Responsibilities · Design, develop and improve upstream and downstream processes for LVVs to deliver robust manufacturing platforms for early and late-stage clinical and commercial development · Execute experimental plans, analyse experimental data and write technical reports · Provide hands-on technical expertise/scientific guidance to team members and supervision of junior colleagues · Contribute to the transfer of improved processes to GMP and assist with oversight of manufacturing activities as required · Assist in the reporting, investigation and resolution of deviations encountered during GMP production activities · Prepare, review and complete protocols/SOPs, study reports and assist with regulatory submissions · Communicate, share and discuss work progress internally and externally · Perform landscape scouting to drive continuous improvement in quality, yield and COGs · Provide expert review and approval of executed batch, records, test records and associated documentation for release of LVVs and plasmids used in their production. Experience & Knowledge · In-depth knowledge of state-of-the-art cell & gene therapy products and available technologies, more specifically regarding viral vectors · Minimum of 5 years of experience with development, manufacture and delivery of viral vectors, preferably retro and lentiviral vectors · Demonstrated skills and hands-on experience in adherent and suspension cell lines in different culture systems · Demonstrated knowledge in designing and developing processes for LVV production and purification · Experience in process characterization and validation of the large-scale cGMP production of lentiviral vectors · Use of more specialist lab equipment e.g. bioreactors, AKTA, TFF systems, etc · Proficiency with MS office, MFCS, SnapGene, Unicorn, e-lab books and other commonly used software is required. Experience with DoE software (s) and statistical analysis would be ideal. · Understanding of and familiarity with regulatory guidance governing vector-based products is preferred. Skills and Abilities · Ability to operate in a fast paced, multidisciplinary industrial environment · Creativeness, motivation, and troubleshooting skills to solve problems and/or develop new technical capabilities · Excellent interpersonal and communication skills · Ability to independently design and execute experiments following laboratory procedures, appropriately analyse data and provide an interpretation of results · Strong organization and planning skills to prioritise work and meet deadlines · Experience with supervision of team members and oversight of external activities is preferred. Education · PhD, BSc or equivalent in biotechnology, process development, cell and gene therapy, biological sciences, or other relevant scientific discipline. #J-18808-Ljbffr
Principal Scientist, Viral Vector Development employer: Orchard Therapeutics
Contact Detail:
Orchard Therapeutics Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Scientist, Viral Vector Development
✨Tip Number 1
Make sure to highlight your hands-on experience with viral vector development, especially with lentiviral vectors. This role requires a deep understanding of the processes involved, so be prepared to discuss specific projects you've worked on.
✨Tip Number 2
Familiarize yourself with the latest technologies and methodologies in cell and gene therapy. Being able to discuss recent advancements or trends in the field can set you apart during discussions with our team.
✨Tip Number 3
Demonstrate your ability to work in a multidisciplinary environment. Share examples of how you've collaborated with different teams, such as analytics or regulatory, to achieve project goals.
✨Tip Number 4
Prepare to showcase your problem-solving skills. We value creativity and motivation, so think of instances where you've successfully tackled challenges in your previous roles.
We think you need these skills to ace Principal Scientist, Viral Vector Development
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Principal Scientist position. Highlight key responsibilities and required skills that match your experience, especially in viral vector development and gene therapy.
Tailor Your CV: Customize your CV to emphasize relevant experience in developing and manufacturing viral vectors. Include specific examples of projects you've worked on, particularly those involving lentiviral vectors and GMP production.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for gene therapy and your technical expertise. Discuss how your background aligns with Orchard Therapeutics' mission and how you can contribute to their innovative work in viral vector development.
Highlight Technical Skills: In your application, be sure to mention your proficiency with lab equipment and software relevant to the role, such as bioreactors and statistical analysis tools. This will demonstrate your readiness to hit the ground running.
How to prepare for a job interview at Orchard Therapeutics
✨Showcase Your Technical Expertise
Be prepared to discuss your in-depth knowledge of viral vectors and gene therapy products. Highlight specific projects where you developed or improved processes for LVV production, and be ready to explain the methodologies you used.
✨Demonstrate Problem-Solving Skills
Expect questions that assess your troubleshooting abilities. Share examples of challenges you've faced in previous roles and how you creatively resolved them, especially in a fast-paced, multidisciplinary environment.
✨Communicate Effectively
Since this role involves collaboration with various teams, practice articulating your thoughts clearly. Prepare to discuss how you’ve communicated complex scientific concepts to both technical and non-technical stakeholders.
✨Prepare for Regulatory Discussions
Familiarize yourself with regulatory guidance governing vector-based products. Be ready to discuss how you have ensured compliance in past projects and how you would approach regulatory submissions in this role.