Level

Hims & Hers

Senior Scientist, R&D - Assay Development

Hims & Hers is hiring a Senior Scientist, R&D - Assay Development. It pays $125k-$140k a year and Level rates it ; you can apply on Hims & Hers.

Level's read on this job

  • Level rates this role Little AI ●○○○: aI is not part of the work.
  • Tools and skills the posting cites include Elisa, Lc Ms Ms and assay development.
  • Level classifies it as a senior role.
  • Level lists 150 other open roles at Hims & Hers.

AI in this role

Senior research and development scientist designing and validating diagnostic assays for clinical testing programs.

elisalc-ms-ms
assay-developmentmethod-validationdesign-of-experimentsclinical-chemistry

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we’re making better health outcomes easier to achieve. 

Hims & Hers is a public company, traded on the NYSE under the ticker symbol “HIMS.” To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company’s outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit www.hims.com/careers-professionals.

About the Role:

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 YourBio 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

We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to apply—even if you're not sure if your background or experience is a perfect match.

Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Hims & Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at accommodations@forhims.com and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims & Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address.

To learn more about how we collect, use, retain, and disclose Personal Information, please visit our Global Candidate Privacy Statement.

How we rate this

Senior Scientist, R&D - Assay Development at Hims & Hers rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Assay DevelopmentMethod ValidationDesign Of ExperimentsClinical ChemistryElisaLc Ms Ms

Questions you could be asked

  1. Tell me about a project where assay development was part of your work. What did you do?
  2. Tell me about a project where method validation was part of your work. What did you do?
  3. Tell me about a project where design of experiments was part of your work. What did you do?
  4. Tell me about a project where clinical chemistry was part of your work. What did you do?
  5. Walk me through how you've used Elisa in your day-to-day work.

Adapt your resume

  • List these exact terms on your resume: Assay Development, Method Validation, Design Of Experiments, Clinical Chemistry, and Elisa. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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