Principal Research Scientist I, Lipid Design and Formulations Development
Company: Abbvie
Location: San Diego
Posted on: January 12, 2026
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Job Description:
Company Description AbbVie's mission is to discover and deliver
innovative medicines and solutions that solve serious health issues
today and address the medical challenges of tomorrow. We strive to
have a remarkable impact on people's lives across several key
therapeutic areas immunology, oncology, neuroscience, and eye care
and products and services in our Allergan Aesthetics portfolio. For
more information about AbbVie, please visit us at www.abbvie.com .
Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and
Tik Tok . Job Description Overview We are seeking a highly
motivated and innovative Formulation Scientist to join our LNP
development team. In this role, you will be responsible for leading
projects focused on lipid design, formulation development, and
characterization of targeted LNP drug products to support internal
platform and pipeline programs. The ideal candidate will have a
deep understanding of LNP formulation and lipid chemistry,
analytical characterization and functional screening in vitro and
in vivo. Responsibilities Independently lead research efforts
through deep technical understanding and work collaboratively
within a cross-functional product development team to drive design,
functional screening, development and production of novel tLNP
formulations for targeted, extra hepatic delivery of nucleic acid
payloads. Discover and optimize novel lipid designs and
applications from diverse structural families for LNP platform
technology development Collaborate with various groups across the
organization including mRNA, analytical, conjugation, antibody and
CMC process development groups to advance pipeline programs
Routinely act as a group leader on formulation projects and provide
mentorship to a small group of research associates. Contribute to
formulations/process development sections of regulatory filings
(IND, NDA etc.) Review scientific literature, patents, scientific
abstracts to stay up to date on latest in the field. Provide
scientific expertise in the organization with special emphasis on
lipid nanoparticle-based drug targeting delivery systems for
nucleic acids Qualifications BS or equivalent education and
extensive, typically 14 years of industry experience; MS or
equivalent education with typically 12 years of industry
experience; PhD with typically 6 years of industry experience in
scientific area of discipline. Preferred: PhD in Chemistry,
Biochemistry, Bioengineering, or Pharmaceutical Sciences with
experience in the design and development of nanoparticle-based drug
delivery systems or complex biologics. Deep technical prowess is
required with respect to lipid chemistry and LNP formulation.
Demonstrated ability to establish new capabilities and innovate
strategies in pursuit of scientific excellence. Must possess in
depth understanding of all aspects of formulation development as
well as downstream characterization including physicochemical,
stability and biological evaluation. Experience with process: lipid
nanoparticle formulation and purification processes, and/or
experience with process development, scale-up/out, engineering and
GMP manufacturing of biologic drug product processes are highly
desired. Experience with supervision, mentorship, or training of
other team members. Good track record of scientific publications
and patents in the field of lipid nanoparticle-based drug delivery
systems is desired Must be an independent thinker with a passion
for developing novel formulation technologies. Experience in
contributing to formulation and pharmaceutical development sections
of regulatory filings is highly desirable. Details oriented with
good organization skills, great troubleshooting skills, team
player, excellent oral and written communication skills are
necessary for this position. Additional Information Applicable only
to applicants applying to a position in any location with pay
disclosure requirements under state orlocal law: The compensation
range described below is the range of possible base pay
compensation that the Companybelieves ingood faith it will pay for
this role at thetimeof this posting based on the job grade for this
position.Individualcompensation paid within this range will depend
on many factors including geographic
location,andwemayultimatelypaymore or less than the posted range.
This range may bemodifiedin thefuture. We offer a comprehensive
package of benefits including paid time off (vacation, holidays,
sick),medical/dental/visioninsurance and 401(k) to
eligibleemployees. This job is eligible toparticipatein our
short-term incentiveprograms. Note: No amount of payis considered
to bewages or compensation until such amount is earned, vested,
anddeterminable.The amount and availability of anybonus,commission,
incentive, benefits, or any other form ofcompensation and
benefitsthat are allocable to a particular employeeremainsin the
Company's soleandabsolutediscretion unless and until paid andmay
bemodifiedat the Companys sole and absolute discretion, consistent
withapplicable law. AbbVie is an equal opportunity employer and is
committed to operating with integrity, driving innovation,
transforming lives and serving our community. Equal Opportunity
Employer/Veterans/Disabled. US & Puerto Rico only - to learn more,
visit
https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation,
click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Keywords: Abbvie, Downey , Principal Research Scientist I, Lipid Design and Formulations Development, Science, Research & Development , San Diego, California