Johnson & Johnson

Principal Scientist, Vector Biology

Johnson & Johnson$117K — $201K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in relevant fields (Cell Biology, Molecular Biology, Virology, Biochemistry, Biomedical Engineering) or equivalent experience
  • 3-6 years of industry experience leading projects or teams
  • Expertise in mammalian cell culture and engineering cell lines
  • Experience developing quantitative cell-based assays for membrane proteins
  • Knowledge of viral entry biology and experimental design
  • Experience with lentiviral vectors and transduction workflows
  • Strong data analysis and communication skills.

Responsibilities

  • Lead research on mechanisms of enveloped virus entry
  • Design and execute experiments on viral glycoprotein and host receptor interactions
  • Develop and validate cell-based assays for receptor localization and virus binding
  • Utilize lentiviral vectors to study cell transduction
  • Establish workflows and quality control measures
  • Integrate data with cross-functional teams for various improvements
  • Present research findings at scientific meetings

Benefits

  • 401(k) and pension plan participation
  • Generous vacation time (120 hours per year)
  • Sick time with varying allowances based on location
  • Parental leave of 480 hours following childbirth or adoption
  • Structured bereavement and caregiver leave policies
  • Volunteer leave allowance of 32 hours per year
  • Military spouse time-off available
Full Job Description
Job Function:
Discovery & Pre-Clinical/Clinical Development

Job Sub Function:
Biological Research

Job Category:
Scientific/Technology

All Job Posting Locations:
Cambridge, Massachusetts, United States of America

Job Description:

We are searching for the best talent for a Principal Scientist, Vector Biology to be in Cambridge, MA.

Purpose:

We are seeking a Principal Scientist to spearhead receptor and viral-entry biology initiatives that translate mechanistic insight into therapeutic progress. Responsibilities include creating and validating cell-based assays for receptor localization and ligand/virus binding, dissecting entry pathways, and optimizing lentiviral transduction in coordination with cross-functional teams.

You will be responsible for:
  • Lead and contribute to research focused on the cellular and molecular mechanisms of enveloped virus entry.
  • Design and execute experiments to characterize the interactions between viral glycoproteins and host cell receptors.
  • Design, develop, and validate robust cell-based assays probing: receptor expression/localization and ligand/virus binding; internalization/endocytosis pathways; functional readouts by flow cytometry, high-content/fluorescence microscopy, and reporter assays.
  • Utilize lentiviral vector systems to study the transduction of target cells and to develop novel gene delivery platforms.
  • Establish scalable, reproducible workflows and SOPs; implement assay performance criteria and QC.
  • Integrate data with cross-functional partners (protein/vector engineering, analytics, translational, process/CMC) to inform target selection, vector design, and process improvements.
  • Present research findings at internal and external scientific meetings


Qualifications:
  • PhD in Cell Biology, Molecular Biology, Virology, Biochemistry, Biomedical Engineering or related field (or equivalent industry experience)
  • 3-6 years of relevant industry experience with a record of leading scientific projects and/or teams.
  • Deep hands-on expertise in mammalian cell culture and cell line engineering.
  • Proven track record developing and running quantitative cell-based assays for membrane proteins/receptors (e.g., flow cytometry panels, internalization assays, high-content imaging).
  • Practical knowledge of viral entry biology (receptor-ligand interactions; endocytic/internalization mechanisms) and ability to design mechanistic experiments.
  • Direct experience with lentiviral vectors and transduction workflows, including assay development and optimization in cell lines and/or primary cells.
  • Strong data analysis and scientific communication skills; demonstrated ability to drive decisions with clear, reproducible results.
  • Experience with pseudovirus or live-virus entry/neutralization assays under BSL2/BSL2+ preferred
  • High-throughput/automated assay development, liquid handling, and/or screening experience a plus
  • Record of publications/patents in receptor biology, viral entry, or vector technologies.

Required Skills:

Preferred Skills:
Big Data Management, Critical Thinking, Data Reporting, Data Savvy, Drug Discovery Development, Molecular Diagnostics, Organizing, Pharmaceutical Microbiology, Problem Solving, Product Knowledge, Project Reporting, Project Schedule, Research Proposals, Scientific Research, Standard Operating Procedure (SOP), Standard Scientific Processes and Procedures, Strategic Thinking, Sustainability

The anticipated base pay range for this position is :
$117,000.00 - $201,250.00

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)).

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

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
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