Senior Scientist, Translational Systems Toxicology
- J&J Family of Companies
- San Diego, California
- Full Time
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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
**Job Function:**
Discovery & Pre-Clinical/Clinical Development
**Job Sub** **Function:**
Nonclinical Safety
**Job Category:**
Scientific/Technology
**All Job Posting Locations:**
San Diego, California, 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
**We are searching for the best talent for a** **Senior Scientist, Translational Systems Toxicology** **to be onsite in La Jolla, CA.**
**Purpose:**
The Senior Scientist, Translational Systems Toxicology, will be part of the multi-disciplinary Translational Safety team in Preclinical Sciences and Translational Safety (PSTS) and will have first-hand involvement in the drug discovery process, from inception to clinic and beyond. This candidate will have an established track record using bioanalytical instrumentations primarily on proteomics and/or imaging mass spectrometry, with strong experience handling various cell and tissues samples.
**You will be responsible for** **:**
+ Thoughtfully implement various arts of mass spectrometry (e.g., applying imaging, TOF, Orbitrap etc in both global and targeted acquisition modes) to support projects of multiple drug modalities such as small molecules, siRNA, PROTAC, Bispecific antibody, and CAR T-cell therapy.
+ De novo methodology design and productive implementation, for studies using mass spectrometry, to ensure timely delivery.
+ Initiate and perform hypothesis-driven investigation into mechanisms of toxicities.
+ Work closely and be an avid contributor within the multi-disciplinary Translational Safety team to leverage expertise in cell & molecular biology, computational chemistry and biology.
+ Be part of the evidence generation group by working closely with pathologists, toxicologists, DMPK and in vivo scientists to aid regulatory submissions and mitigate toxicology findings.
+ Communicate study results and provide guidance to stakeholders in applying those results toward strategic decisions.
**Qualifications / Requirements:**
**Education:**
+ Minimum of a Bachelors degree is required
+ Advanced degree (Master's, PhD) in biochemistry, analytical chemistry or a related field is highly preferred
**Required:**
+ Minimum 4-6 years of experience in the pharmaceutical industry/academia setting
+ Able to independently design and perform proteomic approaches across different experiment types (global proteomic profiling, PTM, targeted and affinity MS analysis) using a variety of sample sources.
+ Experience with several MS acquisition modes (e.g., DDA, DIA, PRM, MRM) and proteomic software.
+ A track record of de novo mass spectrometry methodology design for both small and large molecules in complex biological samples.
+ Proven record of scientific curiosity, creative thinking and a deep understanding of biology.
+ Strong self-motivation and drive to make impactful contributions.
+ Excellent analytical, communication and collaboration skills.
+ Travel up to 10%, defined by business needs
**Preferred:**
+ Demonstrated project team experience at a pharmaceutical company and ability to work effectively in a matrix, global environment as part of a multidisciplinary team.
+ Ability to leverage large omics data sets
+ First-hand experience with cell cultures (e.g., organoid & iPSC)
+ Imaging mass spectrometry experiences
+ Maintaining and troubleshooting nano/micro-flow liquid chromatography systems
+ Broad toxicology and pre-clinical safety expertise. Experiences with biochemical, molecular and cellular biology techniques.
The anticipated base pay range for this position in the US is $105,000 to $169,050.
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 corporations performance over a calendar/ performance year. Bonuses are awarded at the Companys discretion on an individual basis.
Employees and/or eligible dependents may be 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.
Employees may be eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).
Employees are eligible for the following time off benefits:
+ Vacation - up to 120 hours per calendar year
+ Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year
+ Holiday pay, including Floating Holidays - up to 13 days per calendar year
+ Work, Personal and Family Time - up to 40 hours per calendar year
For additional general information on company benefits, please go to:
This job posting is anticipated to close on July 31, 2025. The Company may however extend this time-period, in which case the posting will remain available on 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 and 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 email the Employee Health Support Center (...) or contact AskGS to be directed to your accommodation resource.
\#LI-Onsite
**The anticipated base pay range for this position is :**
$105,000-$169,050
Additional Description for Pay Transparency:
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 Companys consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Companys 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 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 Condolence Leave 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave 10 days Volunteer Leave 4 days Military Spouse Time-Off 80 hours Additional information can be found through the link below.
**Job Function:**
Discovery & Pre-Clinical/Clinical Development
**Job Sub** **Function:**
Nonclinical Safety
**Job Category:**
Scientific/Technology
**All Job Posting Locations:**
San Diego, California, 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
**We are searching for the best talent for a** **Senior Scientist, Translational Systems Toxicology** **to be onsite in La Jolla, CA.**
**Purpose:**
The Senior Scientist, Translational Systems Toxicology, will be part of the multi-disciplinary Translational Safety team in Preclinical Sciences and Translational Safety (PSTS) and will have first-hand involvement in the drug discovery process, from inception to clinic and beyond. This candidate will have an established track record using bioanalytical instrumentations primarily on proteomics and/or imaging mass spectrometry, with strong experience handling various cell and tissues samples.
**You will be responsible for** **:**
+ Thoughtfully implement various arts of mass spectrometry (e.g., applying imaging, TOF, Orbitrap etc in both global and targeted acquisition modes) to support projects of multiple drug modalities such as small molecules, siRNA, PROTAC, Bispecific antibody, and CAR T-cell therapy.
+ De novo methodology design and productive implementation, for studies using mass spectrometry, to ensure timely delivery.
+ Initiate and perform hypothesis-driven investigation into mechanisms of toxicities.
+ Work closely and be an avid contributor within the multi-disciplinary Translational Safety team to leverage expertise in cell & molecular biology, computational chemistry and biology.
+ Be part of the evidence generation group by working closely with pathologists, toxicologists, DMPK and in vivo scientists to aid regulatory submissions and mitigate toxicology findings.
+ Communicate study results and provide guidance to stakeholders in applying those results toward strategic decisions.
**Qualifications / Requirements:**
**Education:**
+ Minimum of a Bachelors degree is required
+ Advanced degree (Master's, PhD) in biochemistry, analytical chemistry or a related field is highly preferred
**Required:**
+ Minimum 4-6 years of experience in the pharmaceutical industry/academia setting
+ Able to independently design and perform proteomic approaches across different experiment types (global proteomic profiling, PTM, targeted and affinity MS analysis) using a variety of sample sources.
+ Experience with several MS acquisition modes (e.g., DDA, DIA, PRM, MRM) and proteomic software.
+ A track record of de novo mass spectrometry methodology design for both small and large molecules in complex biological samples.
+ Proven record of scientific curiosity, creative thinking and a deep understanding of biology.
+ Strong self-motivation and drive to make impactful contributions.
+ Excellent analytical, communication and collaboration skills.
+ Travel up to 10%, defined by business needs
**Preferred:**
+ Demonstrated project team experience at a pharmaceutical company and ability to work effectively in a matrix, global environment as part of a multidisciplinary team.
+ Ability to leverage large omics data sets
+ First-hand experience with cell cultures (e.g., organoid & iPSC)
+ Imaging mass spectrometry experiences
+ Maintaining and troubleshooting nano/micro-flow liquid chromatography systems
+ Broad toxicology and pre-clinical safety expertise. Experiences with biochemical, molecular and cellular biology techniques.
The anticipated base pay range for this position in the US is $105,000 to $169,050.
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 corporations performance over a calendar/ performance year. Bonuses are awarded at the Companys discretion on an individual basis.
Employees and/or eligible dependents may be 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.
Employees may be eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).
Employees are eligible for the following time off benefits:
+ Vacation - up to 120 hours per calendar year
+ Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year
+ Holiday pay, including Floating Holidays - up to 13 days per calendar year
+ Work, Personal and Family Time - up to 40 hours per calendar year
For additional general information on company benefits, please go to:
This job posting is anticipated to close on July 31, 2025. The Company may however extend this time-period, in which case the posting will remain available on 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 and 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 email the Employee Health Support Center (...) or contact AskGS to be directed to your accommodation resource.
\#LI-Onsite
**The anticipated base pay range for this position is :**
$105,000-$169,050
Additional Description for Pay Transparency:
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 Companys consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Companys 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 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 Condolence Leave 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave 10 days Volunteer Leave 4 days Military Spouse Time-Off 80 hours Additional information can be found through the link below.
Job ID: 486836844
Originally Posted on: 7/25/2025
Want to find more Chemistry opportunities?
Check out the 16,491 verified Chemistry jobs on iHireChemists
Sign Up for Job Alerts
