×
Register Here to Apply for Jobs or Post Jobs. X

Sr. Engineer, Design Quality Assurance

Remote / Online - Candidates ideally in
Minnetonka, Hennepin County, Minnesota, 55345, USA
Listing for: hims & hers
Full Time, Remote/Work from Home position
Listed on 2026-08-24
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer, Process Engineer
Salary/Wage Range or Industry Benchmark: 110000 - 140000 USD Yearly USD 110000.00 140000.00 YEAR
Job Description & How to Apply Below

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  and  . For information on the company’s outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit

About the Role:

The Sr. Design Assurance Engineer, reporting to the Director of Device Quality, supports sustaining and new product design and development activities and ensures the effective transfer of new products into manufacturing. We are looking for a strong engineer who enjoys working in a fast paced and rapidly growing environment where taking initiative and collaborating cross-functionally are critical for success.

You Will:
  • Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
  • Acts as an effective team member in supporting quality disciplines, decisions, and practices.
  • Work within a cross-functional team to identify and implement effective controls for realization of Class II medical devices.
  • Write various technical documentation for procedure execution, technical rationale, and evidence of the development process.
  • Support Design Assurance activities as related to Risk Management, Design Controls, and other DA related priorities.
  • Support Post Market activities, as necessary, of risk based on post-market signals.
  • Actively participate in the Design Change process to ensure the proposed changes to the products are systemically and thoroughly analyzed and assessed.
  • Demonstrate good working knowledge and application of validation and statistical techniques in compliance with associated regulatory requirements and internal standards.
  • Support the verification, validation, and usability testing to meet or exceed internal and external requirements.
  • Develop, update, and maintain Design History File and Design Input / Output documentation (Product Specification, Component Specifications, and Prints).
  • Generate, update, and maintain product risk management tools (e.g., Hazard Analysis, Fault Tree, FMEAs).
  • Partner with R&D to determine and implement Design Controls based on Risk Management, Customer Needs, and Manufacturing Input.
  • Partner cross-functionally to identify and support value improvement efforts to support business goals.
You Have:
  • Minimum of a bachelor’s degree in mechanical or biomedical engineering (or other related technical discipline).
  • 5 - 8+ years of experience in design assurance, new product development or related medical device / regulated industry experience.
  • Self-motivated with a passion for solving problems and a bias for action.
  • Strong communication skills (verbal & written).
  • Demonstrated use of Quality tools/methodologies.
  • Ability to effectively work and collaborate in a mixed onsite + remote environment.
  • Demonstrated experience creating detailed technical documents.
Preferred Qualifications:
  • Experience in development and/or manufacturing of Class II medical devices
  • ISO 13485, ISO 14971 and Quality System Regulations understanding with a focus on Design Controls and Risk Analysis.
  • Experienced problem solver, capable of facilitating the problem-solving process.
  • Adaptable and effective collaborator in a team environment or in self-directed work.
  • Experience with design changes, complaint management, and corrective action.
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…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary