Senior Principal Scientist, Translational Safety
Company: 6084-Janssen Research & Development Legal Enti
Location: San Diego
Posted on: April 1, 2026
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Job Description:
At Johnson & Johnson, we believe health is everything. Our
strength in healthcare innovation empowers us to build a world
where complex diseases are prevented, treated, and cured, where
treatments are smarter and less invasive, and solutions are
personal. Through our expertise in Innovative Medicine and MedTech,
we are uniquely positioned to innovate across the full spectrum of
healthcare solutions today to deliver the breakthroughs of
tomorrow, and profoundly impact health for humanity. Learn more at
jnj.com As guided by Our Credo, Johnson & Johnson is responsible to
our employees who work with us throughout the world. We provide an
inclusive work environment where each person is considered as an
individual. At Johnson & Johnson, we respect the diversity and
dignity of our employees and recognize their merit. Job Function:
Discovery & Pre-Clinical/Clinical Development Job Sub Function:
Nonclinical Safety Job Category: Scientific/Technology All Job
Posting Locations: Cambridge, Massachusetts, United States of
America, San Diego, California, United States of America, Spring
House, Pennsylvania, United States of America Job Description:
About Innovative Medicine Our expertise in Innovative Medicine is
informed and inspired by patients, whose insights fuel our
science-based advancements. Visionaries like you work on teams that
save lives by developing the medicines of tomorrow. Join us in
developing treatments, finding cures, and pioneering the path from
lab to life while championing patients every step of the way. Learn
more at https://www.jnj.com/innovative-medicine We are searching
for the best talent for a Senior Principal Scientist, Translational
Safety to be located in Spring House, PA, Cambridge, MA or San
Diego, CA. Purpose: The Sr. Principal Scientist will serve as a key
member of the Translational Safety team in Translational PK/PD &
Investigative Toxicology (TPPIT) and Preclinical Sciences &
Translational Safety (PSTS) and will be responsible for leading
predictive toxicology initiatives in the early drug discovery and
de-risking. The successful candidate will work in matrixed teams
evaluating, validating, recommending and integrating conventional
in vitro models and complex cellular model systems for predicting
off-target and major organ toxicities and guiding drug candidate
selection during the early drug development process. This scientist
will work closely with teams across PSTS on mechanistic studies as
needed while focusing on moving our predictive toxicity workflows
to the next level. The Distinguished Scientist will be responsible
for communicating predictive investigative screening plans and
updates to PSTS issues teams, project teams, and global leadership
in partnership with leaders in Translational Safety and in
Therapeutic Development. Strong knowledge of AI/ML model
development is essential as we invest in an R&D wide digital
transformation. You will be responsible for: Lead efforts to build
and refine robust high-throughput in vitro organ specific cellular
screening workflows Serve as the liaison between High throughput
screening, Data Sciences, In Silico Modeling and Preclinical Safety
Teams In collaboration with External Scientific Innovation and
Business Development, evaluate external environment to identify new
technologies, platforms & CROs with novel, cutting edge
applications for in vitro toxicology Partner with members of
Translation Safety & Discovery, Product Development and Supply
(DPDS) functional groups to oversee the conversion of mechanistic
cellular, molecular & biochemical toxicology assays into high
throughput predictive screening assays Function as a key member of
Global Translational Safety Team partnering with global leads to
establish strategic goals and objectives Communicate screening
plans and updates to leadership and multidisciplinary teams
Maintain toxicology expertise through collaborations within TPPIT &
PSTS globally, DPDS, and through organizational associations,
literature reviews, continuing education, and publications. Partner
with Global Lead of Cellular & Molecular Toxicology, as well as
Safety Pharmacology leads to establish strategic goals and
objectives. Identify topics appropriate for internal and external
scientific publication, author scientific publications, posters and
or draft documents for official communication (i.e. Contributing
Scientist Reports, weight of evidence packages). Qualifications /
Requirements: Education: A minimum of a Ph.D. and postdoctoral work
in Toxicology, Pharmacology, Biology or related field is required.
Skills/Experience: A minimum of 2 years postdoctoral training and 6
years of relevant work experience is required. Demonstrated
knowledge in designing and conducting mechanistic in vitro studies
incorporating high throughput applications of cell-based models
required. Experience with high throughput applications of
organotypic models incorporating multiple cell types including
immune cells required. Demonstrated knowledge of drug discovery and
experience with drug modalities beyond small molecules required.
Advanced knowledge of cellular and molecular toxicology and
demonstrated experience driving projects to completion required.
Track record of working collaboratively to solve sophisticated
scientific problems required. Experience working on & leading
highly matrixed, multi-disciplinary teams required. Experience with
AI/ML and in silico toxicology modeling preferred. Board
Certification in Toxicology preferred. Must be highly motivated,
curious, and organized individual with a team-oriented mentality
who enjoys working in a fast-paced, dynamic environment, and
working collaboratively across functions. Excellent written,
visual, and oral communication skills. The expected pay range for
this position is $137,000 to $235,750. The Company maintains highly
competitive, performance-based compensation programs. Under current
guidelines, this position is eligible for an annual performance
bonus in accordance with the terms of the applicable plan. The
annual performance bonus is a cash bonus intended to provide an
incentive to achieve annual targeted results by rewarding for
individual and the corporation’s performance over a calendar/
performance year. Bonuses are awarded at the Company’s discretion
on an individual basis. Subject to the terms of their respective
plans, employees and/or eligible dependents are eligible to
participate in the following Company sponsored employee benefit
programs: medical, dental, vision, life insurance, short and
long-term disability, business accident insurance, and group legal
insurance. Subject to the terms of their respective plans,
employees are eligible to participate in the Company’s consolidated
retirement plan (pension) and savings plan (401(k)). This position
is eligible to participate in the Company’s long-term incentive
program. Subject to the terms of their respective policies and date
of hire, employees are eligible for the following time off
benefits: Vacation –120 hours per calendar year Sick time - 40
hours per calendar year; for employees who reside in the State of
Colorado –48 hours per calendar year; for employees who reside in
the State of Washington –56 hours per calendar year Holiday pay,
including Floating Holidays –13 days per calendar year Work,
Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the
birth/adoption/foster care of a child Bereavement Leave – 240 hours
for an immediate family member: 40 hours for an extended family
member per calendar year Caregiver Leave – 80 hours in a 52-week
rolling period10 days Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year For
additional general information on company benefits, please go to:
https://www.careers.jnj.com/employee-benefits This job posting is
anticipated to close on March 21, 2026. The Company may however
extend this time-period, in which case the posting will remain
available on https://www.careers.jnj.com to accept additional
applications. Johnson & Johnson is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment
without regard to race, color, religion, sex, sexual orientation,
gender identity, age, national origin, disability, protected
veteran status or other characteristics protected by federal, state
or local law. We actively seek qualified candidates who are
protected veterans and individuals with disabilities as defined
under VEVRAA and Section 503 of the Rehabilitation Act. Johnson &
Johnson is committed to providing an interview process that is
inclusive of our applicants’ needs. If you are an individual with a
disability and would like to request an accommodation, please
contact us via https://www.jnj.com/contact-us/careers or contact
AskGS to be directed to your accommodation resource. Required
Skills: Preferred Skills: Clinical Data Management, Drug Discovery
Development, EHS Compliance, Emergency Planning, Performance
Measurement, Presentation Design, Process Hazard Analysis (PHA),
Process Optimization, Program Management, Regulatory Affairs
Management, Research and Development, Risk Management, Safety
Audits, Safety Investigations, Safety-Oriented, Scientific
Research, Strategic Thinking, Tactical Planning, Technical
Credibility The anticipated base pay range for this position is :
$137,000.00 - $235,750.00 Additional Description for Pay
Transparency: Subject to the terms of their respective plans,
employees are eligible to participate in the Company’s consolidated
retirement plan (pension) and savings plan (401(k)). This position
is eligible to participate in the Company’s long-term incentive
program. Subject to the terms of their respective policies and date
of hire, employees are eligible for the following time off
benefits: Vacation –120 hours per calendar year Sick time - 40
hours per calendar year; for employees who reside in the State of
Colorado –48 hours per calendar year; for employees who reside in
the State of Washington –56 hours per calendar year Holiday pay,
including Floating Holidays –13 days per calendar year Work,
Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the
birth/adoption/foster care of a child Bereavement Leave – 240 hours
for an immediate family member: 40 hours for an extended family
member per calendar year Caregiver Leave – 80 hours in a 52-week
rolling period10 days Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year For
additional general information on Company benefits, please go to: -
https://www.careers.jnj.com/employee-benefits
Keywords: 6084-Janssen Research & Development Legal Enti, Palm Desert , Senior Principal Scientist, Translational Safety, Science, Research & Development , San Diego, California