Senior Scientist Vector Engineering

AstraZeneca

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profile Job Location:

Waltham, MA - USA

profile Monthly Salary: $ 113902 - 170854
Posted on: 3 days ago
Vacancies: 1 Vacancy

Job Summary

Are you ready to dive into the world of transformative therapies and make a significant impact At EsoBiotec now part of AstraZeneca we are setting new benchmarks for biotechnological research. Our collaboration combines AstraZenecas global influence and scientific innovation with EsoBiotec s unique culture of creativity and breakthroughs in cell-based therapies and immunology. Here your scientific passion will drive real-world impact as you contribute to life-changing are looking for an inspiring Senior Scientist Vector Engineering to drive innovation and development of our pioneering lentiviral vector therapeutic platform. Join us in shaping the future of cell and gene therapy with your expertise in viral vector engineering gene editing CAR and TCR T cell engineering or myeloid immunobiology in cancer.

Responsibilities

  • Design build and validate novel lentiviral vectors for in vivo cell therapy applications.

  • Perform hands-on construct designs viral genome optimization viral envelope pseudotype engineering and vector assembly.

  • Design plan and execute in vitro and in vivo experiments to assess transduction efficiency specificity expression durability and safety profile of novel in vivo LVVs.

  • Develop and run assays for titer potency biodistribution integration site analysis and immunogenicity in collaboration with analytics partners.

  • Apply literature mining public datasets and personal expertise to generate innovative testable hypotheses and prioritize vector concepts.

  • Implement rigorous experimental design statistical analysis and documentation to ensure reproducibility traceability and data integrity.

  • Collaborate extensively with discovery teams across AZ including payload biology bioinformatics and nonclinical to align vector designs with product requirements.

  • Contribute to platform development by creating screening workflows model systems and standardized protocols for vector performance.

  • Present findings risks and recommendations in working groups and project meetings and drive decisions through clear data storytelling.

  • Support IP generation by contributing to invention disclosures and sharing FTO considerations with the IP team.

Essential Skills/Experience

  • PhD in molecular biology virology bioengineering or related field with 4 years of postdoctoral experience in academia or industry.

  • Demonstrated expertise in viral vectors and virology with a strong track record in viral vector design engineering and characterization for gene therapy

  • Proficiency in molecular biology techniques for vector construction promoter and regulatory element engineering and payload optimization.

  • Experience in protein and antibody (scFV and VHH) engineering or envelope/pseudotype modification to tune tropism entry and transduction profiles.

  • Hands-on familiarity with in vitro cell culture assays and in vivo models for vector evaluation including transduction assays doseresponse durability studies and safety readouts.

  • Strong hands-on competence with quantitative analytics such as flow cytometry and qPCR/ddPCR.

  • Ability to design rigorous experiments apply statistics and interpret complex datasets to drive go/no-go decisions.

  • Strong collaboration and communication skills to operate as a backbone member of cross-functional working groups and align discovery efforts with product goals.

  • Evidence of innovation through publications presentations or open-source contributions and comfort leveraging literature and public data to ideate and de-risk.

  • Organized proactive and product-focused mindset with the ability to manage multiple experiments meet timelines and maintain high-quality documentation.

  • Commitment to being fully hands-on at the bench while mentoring peers and contributing to platform and program deliverables.

Desirable Skills/Experience

  • Strong preference for lentiviral vectors.

  • Practical understanding of safety risks and mitigations for LVV including insertional mutagenesis off-target transduction immunogenicity and RCL testing.

When we put unexpected teams in the same room we fuel bold thinking with the power to inspire life-changing -person working gives us the platform we need to connect work at pace and challenge perceptions. Thats why we work on average a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and daring world.

The annual base pay for this position ranges from $113902 - $170854 USD Annual. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors including market location job-related knowledge skills and addition our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles) to receive a retirement contribution (hourly roles) and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program 401(k) plan; paid vacation and holidays; paid leaves; and health benefits including medical prescription drug dental and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired employee will be in an at-will position and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time including for reasons related to individual performance Company or individual department/team performance and market factors.

Date Posted

18-May-2026

Closing Date

21-May-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and furtherance of that mission we welcome and consider applications from all qualified candidates regardless of their protected characteristics. If you have a disability or special need that requires accommodation please complete the corresponding section in the application form.


Required Experience:

Senior IC

Are you ready to dive into the world of transformative therapies and make a significant impact At EsoBiotec now part of AstraZeneca we are setting new benchmarks for biotechnological research. Our collaboration combines AstraZenecas global influence and scientific innovation with EsoBiotec s unique ...
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AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, ... View more

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