Principal Scientist II, Cell & Gene Therapy Delivery
Company: Advanced Accelerator Applications (Italy) - S...
Location: San Diego
Posted on: October 22, 2024
Job Description:
Principal Scientist II, Cell & Gene Therapy DeliveryJob ID:
REQ-10021278Date: Sep 10, 2024Location: USASummaryPosition is
onsite in San Diego.Summary:INNOVATION, QUALITY, COLLABORATION,
PERFORMANCE, COURAGE AND INTEGRITY.Novartis Biologics Center (BRC)
builds the Novartis biologics pipeline in collaboration with
Biomedical Research disease and functional area departments via a
breadth of technologies for discovery of antibody, protein, cell
and gene therapy-based therapeutics. The Cell and Gene Therapy
(CGT) group within BRC drives a diverse portfolio of modalities
including multi-specific antibodies, CAR-T, RNA therapeutics and
AAV. Through cell and viral engineering as well as innovative and
rational protein design, the CGT group is a global team that works
collaboratively with disease area groups to broaden the use of
biologics into therapeutic applications where conventional
antibodies have limitations.As a Principal Scientist II part of the
BRC CGT group in San Diego, CA, you will have a unique opportunity
to be at the cutting edge of the cell and gene therapy field and
lead and contribute to the development of innovative medicines for
patients devastated by diseases in collaboration with partners
across the global Novartis research and development network.About
the RoleYour responsibilities will include, but are not limited
to:
- Lead, oversee and/or participate in next-generation CGT
delivery improvement projects across multiple Novartis sites to
enable pipeline and platform advances and novel therapeutic
capabilities in close collaboration with disease area leaders and
global project teams.
- Undertake and lead efforts to develop more potent, safer and
tolerable LVV and AAV vectors. The mechanisms in scope include, but
are not limited to, improving tropism/targeting, reduction of
immune response, spatial/temporal regulated expression control
strategies, circuit engineering,
transcriptional/post-transcriptional aspects and strategies for
high throughput optimization of vector components.
- Enable translation from in vitro/in vivo mouse and nonhuman
primate POC studies to therapeutic disease programs for preclinical
development.
- Initiate, lead and contribute to interdisciplinary research
programs in a highly collaborative and matrixed manner across
internal groups and with external partners.
- Prepare reports, manuscripts and protocols, adhering to the
good research practices and quality culture across NIBR. Present
results at appropriate internal and external meetings and
conferences.
- Other related duties as assigned.What you'll bring to the
role:Requirements:
- Bachelor's degree in cell and gene therapy, bioinformatics,
molecular/cell biology, bioengineering, or related scientific field
with 12 years industry or equivalent experience or Master's with
degree in cell and gene therapy, bioinformatics, molecular/cell
biology, bioengineering, or related scientific field with 10 years
industry or equivalent experience or PhD with 6 years of industry
or equivalent experience.
- Successful track record in directly and in a matrix manner
leading scientists and project team members with diverse
backgrounds is required.
- Demonstrated expertise in LVV and AAV biology, virology, viral
tropism engineering, transcriptional and post-transcriptional
mechanisms, and analytical/process development for LVV/AAV
production is required.
- The position requires the ability to work collaboratively
across a dynamic and collaborative scientific and development
environment. Therefore adaptability to emerging project/group
needs, excellent communication skills, both written and verbal, and
strong interpersonal skills are required.
- Strong publication, patent and/or external presentation
record.
- Genetic/epigenomic/transcriptomic profiling technologies,
genome engineering (e.g. CRISPR), nonviral gene therapy, sh/miRNA
biology, and/or analytical/process development for LVV/AAV
production are highly desired.Please note this job description is
not designed to cover or contain a comprehensive listing of
activities, duties or responsibilities that are required of the
employee for this job. Duties, responsibilities and activities may
change at any time with or without notice.Why Novartis: Helping
people with disease and their families takes more than innovative
science. It takes a community of smart, passionate people like you.
Collaborating, supporting and inspiring each other.Commitment to
Diversity & Inclusion: The Novartis Group of Companies are Equal
Opportunity Employers and take pride in maintaining a diverse
environment. We do not discriminate in recruitment, hiring,
training, promotion or other employment practices for reasons of
race, color, religion, gender, national origin, age, sexual
orientation, gender identity or expression, marital or veteran
status, disability, or any other legally protected
status.Accessibility & Reasonable Accommodations: The Novartis
Group of Companies are committed to working with and providing
reasonable accommodation to individuals with disabilities. If,
because of a medical condition or disability, you need a reasonable
accommodation for any part of the application process, or to
perform the essential functions of a position, please send an
e-mail to us.reasonableaccommodations@novartis.com or call
+1(877)395-2339 and let us know the nature of your request and your
contact information. Please include the job requisition number in
your message.Division: Biomedical ResearchBusiness Unit: Pharma
ResearchLocation: USASite: San DiegoCompany / Legal Entity: U175
(FCRS = US175) Novartis Institutes for BioMedical Research,
Inc.
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Keywords: Advanced Accelerator Applications (Italy) - S..., La Mesa , Principal Scientist II, Cell & Gene Therapy Delivery, Healthcare , San Diego, California
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