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Senior Scientist, R&D - Assay Development

Job in South Plainfield, Middlesex County, New Jersey, 07080, USA
Listing for: hims & hers
Full Time position
Listed on 2026-07-19
Job specializations:
  • Research/Development
    Research Scientist, Clinical Research, Medical Technologist & Lab Technician, Biotech Research
Job Description & How to Apply Below

Senior Scientist, R&D

Hims & Hers is seeking a Senior Scientist, R&D to join our growing laboratory organization. This individual contributor will report to the Director of R&D and work closely to develop and validate diagnostic assays supporting both traditional and at-home testing programs, and support assay implementation into clinical operations. The ideal candidate is bench-strong, with hands-on experience across the full assay development lifecycle - from feasibility and optimization through verification and validation;

and thrives in a fast-moving, early-stage environment. This is an on-site laboratory role based in Central New Jersey.

You Will:

Assay Development and Validation

  • Design and execute immunoassay development, optimization, and verification studies including ELISA, chemiluminescent, and multiplex formats
  • Perform method validation experiments including precision, accuracy, linearity, interference, and stability testing per established protocols
  • Apply Design of Experiments (DOE) and statistical methodologies to assay optimization and troubleshooting
  • Support LC-MS/MS method development and validation for clinical chemistry and hormone analytes
  • Evaluate performance characteristics of capillary versus venous specimens, investigate interference, and develop strategies to extend sample stability
  • Develop and revise SOPs to support consistent, reproducible laboratory operations
  • Prepare validation summaries, protocols, and technical reports in compliance with quality and regulatory standards

Laboratory Execution

  • Perform hands-on laboratory testing using specimens collected via at-home devices such as Tasso and Your Bio Health, including whole blood, plasma, serum, and other biological matrices
  • Operate LC-MS/MS instrumentation (SCIEX 4500MD or equivalent) including sample preparation, method validation, and data review
  • Support testing on automated chemistry and hematology platforms including Roche Cobas Pro and Sysmex systems, including CBC and whole blood analyte workflows
  • Support liquid handling automation workflows for sample processing and high-throughput laboratory operations
  • Troubleshoot assay performance issues across immunoassay, clinical chemistry, mass spectrometry, and molecular diagnostic platforms

Data Analysis

  • Analyze experimental data and perform statistical evaluation of assay performance including precision, bias, and total allowable error modeling
  • Prepare figures, tables, and technical summaries for internal review and scientific communication
  • Contribute to peer-reviewed publications and scientific conference presentations

Quality and Regulatory Collaboration

  • Partner with the Quality team to ensure study designs and documentation meet CAP, CLIA, and applicable regulatory requirements
  • Support investigation and resolution of sample rejection issues to improve overall laboratory quality metrics
  • Support laboratory inspection readiness and audit preparation activities
  • Collaborate with Clinical Laboratory Operations during assay transfer and implementation
You Have:
  • PhD in Clinical Chemistry, Biochemistry, Analytical Chemistry, Molecular Biology, or related field with 4+ years; OR Master's degree with 7+ years; OR Bachelor's degree with 10+ years of relevant bench experience in a diagnostic or clinical laboratory setting
  • Demonstrated hands-on experience in immunoassay development including singleplex and multiplex formats
  • Experience with LC-MS/MS instrumentation including sample preparation and method validation
  • Experience with capillary and venous blood-based specimen types
  • Demonstrated experience leading assay validation and verification studies
  • Experience applying DOE and statistical methodologies to assay development and optimization
  • Proven ability to work independently and drive projects from concept to completion

Preferred

  • Experience in a CAP and/or CLIA regulated laboratory environment
  • Experience with at-home or point-of-care diagnostic testing programs
  • Experience with dried blood spot (DBS) workflows and stability characterization
  • Familiarity with emerging biomarker categories relevant to metabolic health, longevity, and consumer wellness testing
  • Experience with NGS-based workflows including library preparation and bioinformatics data review
Our Benefits (there are more but here are some highlights):
  • Competitive salary & equity compensation for full-time roles
  • Unlimited PTO, company holidays, and quarterly mental health days
  • Comprehensive health benefits including medical, dental & vision, and parental leave
  • Employee Stock Purchase Program (ESPP)
  • 401k benefits with employer matching contribution
  • Offsite team retreats
Position Requirements
10+ Years work experience
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