Job description

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 hims.com and hims.com/how-it-works hims.com . 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 hims.com. ABOUT THE ROLE: We are looking for a Senior Product Development Engineer with experience in FDA-regulated devices and packaging development to join our medical device team. You will work hands-on mechanical design of consumer medical devices and the engineering validation of their packaging systems, from concept through design transfer. Your focus is on ensuring the medical device and packaging solutions meet all technical, regulatory, and performance requirements, including strong attention to human factors and usability. Experience with IVD or diagnostic device development is a plus and will be increasingly valuable as our product portfolio grows. This is a hands-on individual contributor role for someone who thrives in a fast-paced environment and is energized by building safe, compliant products that improve people’s lives. YOU WILL: DEVICE & PACKAGING DEVELOPMENT - Hands-on design and development of medical devices, including concept generation, detailed design, prototyping, and design transfer to manufacturing. - Create and maintain design compliant documentation, including design inputs, outputs, DHFs, and engineering change orders. - Execute design verification and validation (V&V) activities, including test protocol authorship, execution, and reporting. - Lead or support human factors engineering (HFE) activities, including use-related risk analysis and formative/summative usability testing. - Apply risk management principles throughout the product development lifecycle. - Develop and evaluate prototypes using appropriate fabrication methods; iterate rapidly based on testing and user feedback. - Support design for production readiness and work with contract manufacturers and suppliers to optimize cost, quality, and scalability. - Evaluate and qualify packaging materials, components, and configurations for device protection, usability, stability, and shipping integrity. - Lead packaging qualification activities including seal strength testing, package integrity testing, and accelerated and real-time aging studies. - Lead or support sterilization validation activities in partnership with external vendors and laboratories. - Coordinate transportation and distribution simulation testing to ensure product integrity through the supply chain. - Maintain complete packaging and device documentation within the DHF and DMR. - Contribute to regulatory submissions through engineering documentation and technical file development. CROSS-FUNCTIONAL & REGULATORY COLLABORATION - Collaborate with Quality, Regulatory Affairs, Operations, Supply Chain, and the Creative Design team to ensure device and packaging readiness for commercialization. - Coordinate testing activities with external laboratories, sterilization vendors, and packaging suppliers. - Assist Regulatory Affairs with submissions and documentation related to device, packaging, and sterilization. - Participate in design reviews, internal audits, supplier assessments, and regulatory inspections as needed. - Contribute to risk management activities related to the device, packaging, shipping, and product transport. YOU HAVE (REQUIRED): - Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Packaging Engineering, or a closely related field. - 8+ years of engineering experience, with a minimum of 4 years in FDA-regulated medical device or diagnostics product development. - Working knowledge of 21 CFR 820 (QSR), ISO 13485, and ISO 11607 quality and packaging standards. - Hands-on experience with design controls, DHF documentation, and design V&V. - Experience authoring and executing packaging qualification or sterilization validation protocols and technical reports. - Experience conducting human factors engineering (HFE) activities per FDA HE75 and IEC 62366-1, including use-related risk analysis and formative/summative usability testing. - Proficiency in SolidWorks or equivalent 3D CAD software; experience with GD&T and tolerance stack-up analysis. - Familiarity with risk management processes per ISO 14971. - Strong written and verbal communication skills for cross-functional collaboration and technical documentation. NICE TO HAVE: - IVD Experience: Experience with diagnostic specimen collection, sample integrity requirements, or diagnostic consumable development (e.g., blood collection, lateral flow, or microfluidic devices). - IVD Experience: Familiarity with CLIA regulations, laboratory interfaces, or point-of-care diagnostic platforms. - Human Factors: Advanced HFE experience including full summative usability study design and execution, moderating use scenarios with target user populations, and generating HFE reports suitable for regulatory submission. - Human Factors: Experience applying IEC 62366-1 and FDA HE75 within a formal design control process, including task analysis, use error identification, and critical task definition. - Experience with Class II or Class III medical devices and exposure to notified body or FDA interaction during submission. 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) - Employee discounts on hims & hers & Apostrophe online products - 401k benefits with employer matching contribution - Offsite team retreats Conditions of Employment: - This position will require working with Hazardous Drugs (HD) and would require that Personal Protective Equipment (PPE) be worn for the length of working with these drugs. These items would include gloves, respiratory protection, gown and other items as required. - This position requires medical approval to wear respiratory protection in the form of negative or positive pressure respirators, including N95, full face respirator, SCBA, or Powered Air Purifying Respirator (PAPR). - Physical exertion required. Including, but not limited to, walking up to 50% of the time, standing up to 100% of the time, squatting and bending up to 20% of the time and lifting up to 80% of the time for up to a twelve hour shift. Must be able to lift up to 50lbs. - Due to the risk of reproductive capability in handling or compounding certain Hazardous Drugs (HD) associates must be willing to confirm that they understand the potential risks (teratogenicity, carcinogenicity and reproductive effects) of handling hazardous drugs. 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 hims.com.

Requirements

Must-haves

Hands-on design and development of medical devices, including concept generation, detailed design, prototyping, and design transfer to manufacturing.
Create and maintain design compliant documentation, including design inputs, outputs, DHFs, and engineering change orders.
Execute design verification and validation (V&V) activities, including test protocol authorship, execution, and reporting.
Lead or support human factors engineering (HFE) activities, including use-related risk analysis and formative/summative usability testing.
Apply risk management principles throughout the product development lifecycle.
Develop and evaluate prototypes using appropriate fabrication methods; iterate rapidly based on testing and user feedback.
Support design for production readiness and work with contract manufacturers and suppliers to optimize cost, quality, and scalability.
Evaluate and qualify packaging materials, components, and configurations for device protection, usability, stability, and shipping integrity.
Lead packaging qualification activities including seal strength testing, package integrity testing, and accelerated and real-time aging studies.
Lead or support sterilization validation activities in partnership with external vendors and laboratories.
Coordinate transportation and distribution simulation testing to ensure product integrity through the supply chain.
Maintain complete packaging and device documentation within the DHF and DMR.
Contribute to regulatory submissions through engineering documentation and technical file development.
Collaborate with Quality, Regulatory Affairs, Operations, Supply Chain, and the Creative Design team to ensure device and packaging readiness for commercialization.

Nice-to-haves

IVD Experience: Experience with diagnostic specimen collection, sample integrity requirements, or diagnostic consumable development (e.g., blood collection, lateral flow, or microfluidic devices).
IVD Experience: Familiarity with CLIA regulations, laboratory interfaces, or point-of-care diagnostic platforms.
Human Factors: Advanced HFE experience including full summative usability study design and execution, moderating use scenarios with target user populations, and generating HFE reports suitable for regulatory submission.
Human Factors: Experience applying IEC 62366-1 and FDA HE75 within a formal design control process, including task analysis, use error identification, and critical task definition.
Experience with Class II or Class III medical devices and exposure to notified body or FDA interaction during submission.
OUR BENEFITS (THERE ARE MORE BUT HERE ARE SOME HIGHLIGHTS):
Competitive salary & equity compensation for full-time roles
Employee Stock Purchase Program (ESPP)
Employee discounts on hims & hers & Apostrophe online products
Offsite team retreats

Application prep

Use the role’s language and application details while tailoring your materials.

Platform: ashby
Effort: quick

Benefits

Benefits detected in the listing.

Dental

Vision

401k

Pto

Parental Leave

Wellness