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Manager, Material Scientist

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Published
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2Application actions
6 Oct 2026Apply before
Opportunity details

About this role.

AI Summary

This is a senior, hands-on pharmaceutical material science leadership role supporting pre-formulation and product development for a healthcare platform. The manager will lead physicochemical characterization, excipient compatibility studies, material qualification, and critical material attribute risk assessments. The role partners closely with R&D, manufacturing, quality, and external analytical or development partners to resolve formulation and scale-up challenges. It also includes people leadership and building durable internal processes and capabilities for material science. The position is remote within the United States with occasional travel.

Role DNA

A quick view of the complexity, pace, ownership and collaboration implied by the job description.

Job Complexity

5/5
EasyHard

Pace & Pressure

4/5
RelaxedFast-paced

Autonomy Level

5/5
GuidedFull ownership

Communication Load

5/5
IndependentCollaborative
AI insightThe role requires deep expertise in pharmaceutical material science, analytical characterization, physical chemistry, and formulation risk management, along with substantial relevant industry experience. It combines technical execution, people management, cross-functional influence, and the creation of new capabilities in an evolving environment.

Salary analysis

Estimated compensation compared with the broader US market for similar roles.

Estimated job medianMarket rate
$150,000
US market range$135k–$175k
AI insightThe disclosed annual base salary range is USD 140,000 to USD 160,000, producing a midpoint of USD 150,000. For a US-based manager-level pharmaceutical material scientist with extensive formulation, pre-formulation, and technical leadership responsibilities, an estimated market range is USD 135,000 to USD 175,000 annually; equity and benefits may be additional.

Core skills

Skills and capabilities most closely associated with this opportunity.

Sample interview questions
How would you design a pre-formulation plan for a new drug substance with uncertain solid-state behavior?

I would begin by defining the target product profile and reviewing available API data. I would then build a risk-based characterization plan covering crystallinity and polymorphism, thermal behavior, particle morphology, solubility across pH, pKa, logP, hygroscopicity, and chemical stability. The findings would be translated into material risks, formulation options, and clear development experiments with decision criteria.

Describe how you approach an excipient compatibility study.

I select excipients based on the intended dosage form, functional need, and known material risks, then use stressed binary or blend studies under appropriate temperature and humidity conditions. I evaluate chemical and physical changes with fit-for-purpose analytical methods such as DSC, XRPD, spectroscopy, and chromatographic stability testing. I interpret results in the context of formulation exposure, processing conditions, and shelf-life requirements before recommending mitigation or alternate excipients.

Tell us about a time you resolved a complex formulation or material-related issue during scale-up or commercial production.

I would first establish a cross-functional problem statement and compare affected and unaffected lots across raw-material attributes, process conditions, and analytical results. I would use structured root-cause tools and targeted experiments to distinguish material variability from process effects. After confirming the cause, I would implement a scalable corrective action, update specifications or controls as needed, and verify that the solution protects product performance.

How do you define and manage critical material attributes for APIs and excipients?

I link material attributes to product quality attributes and process performance through prior knowledge, risk assessment, and experimental data. Attributes such as particle size, polymorphic form, moisture, bulk density, impurity profile, and flow properties are prioritized based on impact and uncertainty. I then establish scientifically justified specifications, supplier controls, incoming testing, and change-management expectations.

How would you lead a technical team while remaining hands-on in a fast-changing R&D environment?

I would set clear technical priorities tied to program milestones, define ownership and decision rights, and use regular reviews to remove barriers. I would remain directly engaged in high-risk scientific questions while coaching team members to design experiments, interpret data, and communicate recommendations independently. Transparent documentation and active alignment with manufacturing, quality, and leadership would keep execution moving as priorities shift.

This analysis is generated from the job description. Salary estimates, role characteristics and sample answers are guidance, not employer-provided facts.

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 Health, Inc. (better known as Hims & Hers) is looking for an experienced Manager, Material Scientist to support and scale our research and development capabilities. This role will partner closely with the VP of R&D and Innovation to help build and lead material science and pre-formulation efforts, while establishing the infrastructure needed to support continued product innovation and growth.

The Manager will play a critical role in bridging early-stage drug concepts with final formulations, supporting the developability of new and existing products. This includes physicochemical characterization, excipient compatibility, and material risk assessment to ensure quality, stability, and scalability across our portfolio.

You will serve as a key subject matter expert in pre-formulation and material science, helping to shape how these capabilities evolve at Hims & Hers. This is a highly hands-on role with a strong focus on technical execution, while also contributing to longer-term capability building.

You’ll work across a range of dosage forms and product types, supporting both new product development and improvements to existing formulations. This role offers the opportunity to contribute to bringing new products from concept through development and into market.

This is a remote role with occasional travel.

You Will:

  • Lead physicochemical characterization of drug substances using techniques such as X-ray diffraction (XRD), DSC/TGA, Raman spectroscopy, and SEM to better understand material properties and behavior

  • Evaluate key drug properties including solubility (pH profile), pKa, logP, and hygroscopicity to inform formulation strategy and product performance

  • Design and interpret excipient compatibility studies to identify potential chemical or physical interactions and ensure product stability and shelf life

  • Partner cross-functionally with R&D, manufacturing, quality, and other teams to address formulation and process challenges across development and production

  • Manage relationships with external partners supporting analytical testing, product development, due diligence, and innovation initiatives

  • Support material qualification efforts, including defining and evaluating specifications for APIs, excipients, vitamins, and minerals

  • Design and implement risk assessments for critical material attributes (CMAs) to ensure consistent product quality and performance

  • Troubleshoot formulation and material-related issues across both development and commercial settings, identifying effective and scalable solutions

  • Contribute to building internal capabilities, processes, and best practices within pre-formulation and material science

You Have:

  • Bachelor’s, Master’s, or PhD in Materials Science, Chemistry, Pharmaceutical Sciences, or a related field, with relevant experience in R&D and/or product development (Bachelor’s: 10–15+ years, Master’s: 5–10+ years, PhD: 5+ years)

  • 2–5+ years of prior people management experience, with the ability to lead and develop technical teams

  • Strong background in material characterization techniques and analytical methods used in pharmaceutical development

  • Deep understanding of physical chemistry, thermodynamics, and drug material properties, including experience applying Biopharmaceutical Classification System (BCS) principles

  • Experience solving complex material or drug performance challenges across development or production environments

  • Experience working cross-functionally to support product development, improvement, and troubleshooting efforts

  • Strong interpersonal and communication skills, with the ability to collaborate effectively across teams and with external partners

  • Comfortable working in a fast-paced, evolving environment with shifting priorities

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.

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This job listing has been manually reviewed by the Jobicy Trust & Safety Team for compliance with our posting guidelines, including verification of the company's legitimacy, accuracy of job details, clarity of remote work policy, and absence of misleading or fraudulent content.

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