Sr. Process & Operations Engineer

Hims & Hers; Menlo Park (CA); On-site; USD 180,000 - 240,000; Full time

Benefits offered by this job

Competitive compensation

Unlimited PTO

Health benefits

ESPP

Employee discounts

401k

Job summary

Hims & Hers in Menlo Park, CA, is seeking a Senior Process / Operations Engineer – Regulated Devices to oversee contract manufacturing for a Class II FDA-regulated medical device. You will coordinate with cross-functional teams, manage CMOs, validate processes, and drive continuous improvement while ensuring quality and regulatory compliance under GMP and ISO 13485.

The role requires strong experience in process engineering within regulated manufacturing environments and collaboration across

Qualifications

• 8+ years of experience in process/operations/manufacturing engineering in the medical device or diagnostics industry.
• Experience supporting Class II FDA-regulated medical devices in a GMP manufacturing environment.
• Direct experience managing or working closely with Contract Manufacturing Organizations (CMOs).

Responsibilities

• Oversee external contract manufacturers and critical suppliers.
• Lead process development, validation, and deployment with R&D and QA.
• Ensure manufacturing quality, regulatory compliance, and cost targets.
• Collaborate with Regulatory, Quality, and Supply Chain for product launches.

Skills

Process engineering

Operations engineering

Manufacturing engineering

CMO management

Education

Bachelor’s degree in Engineering

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 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:

The Senior Process / Operations Engineer – Regulated Devices is responsible for overseeing contract manufacturing operations for a Class II FDA-regulated medical device used for capillary blood collection from a patient’s upper arm into a collection tube for laboratory diagnostic analysis.

This role serves as the primary operational and technical liaison between internal teams and Contract Manufacturing Organizations (CMOs), ensuring manufacturing processes, product quality, and operational performance meet all regulatory, quality, and business requirements. The senior engineer will work cross-functionally with R&D, Quality, Regulatory Affairs, Supply Chain, and external manufacturing partners to support product commercialization, process scalability, validation, and continuous improvement initiatives.

The ideal candidate has strong experience in medical device process engineering, supplier/CMO management, and regulated manufacturing environments with a deep understanding of FDA and ISO quality system requirements.

You Will:

Contract Manufacturing Oversight

• Serve as the primary technical operations lead for external contract manufacturers and critical suppliers
• Oversee day-to-day manufacturing performance, quality metrics, and operational execution at CMOs
• Ensure manufacturing processes consistently meet product specifications, quality standards, and production targets
• Drive accountability with manufacturing partners regarding timelines, deviations, CAPAs, and continuous improvement initiatives

Process Engineering & Manufacturing Support

• Develop, optimize, and sustain manufacturing processes for Class II medical devices and consumables
• Partner with R&D during product development and design transfer activities to ensure manufacturability and scalability
• Support process characterization, validation, and verification activities, including: o IQ/OQ/PQ validation
• Process capability studies
• Equipment qualification
• Manufacturing line readiness
• Lead root cause investigations and implementation of corrective and preventive actions (CAPAs) related to manufacturing or process issues
• Monitor process performance and identify opportunities for yield improvement, cost reduction, and operational efficiency

Quality & Regulatory Compliance

Ensure all manufacturing activities comply with:

• FDA Quality System Regulations (21 CFR Part 820)
• ISO 13485
• GMP requirements
• Internal quality system procedures
• Collaborate closely with Quality Assurance to address nonconformances, deviations, change controls, and audit findings
• Support supplier qualification, supplier audits, and ongoing supplier quality management activities
• Ensure manufacturing documentation, Device History Records (DHRs), and validation records are complete and compliant

Cross-Functional Collaboration

• Work closely with R&D teams to transition new products from development into commercial manufacturing
• Partner with Supply Chain and Planning teams to support production schedules, inventory management, and demand planning
• Support Regulatory Affairs with manufacturing-related documentation for regulatory submissions and inspections
• Coordinate with Packaging, Sterilization, and Logistics teams to ensure seamless product release and shipment readiness

Operational Excellence

• Establish and monitor KPIs related to manufacturing quality, throughput, scrap, and supplier performance
• Drive continuous improvement initiatives using Lean, Six Sigma, or similar methodologies
• Support implementation of scalable operational processes as the company grows
• Assist in risk assessments and mitigation activities related to manufacturing and supply continuity

You Have:

• Bachelor’s degree in Engineering (Mechanical, Biomedical, Industrial, Manufacturing, or related field)
• 8+ years of experience in process engineering, operations engineering, or manufacturing engineering within the medical device or diagnostics industry
• Experience supporting Class II FDA-regulated medical devices in a GMP manufacturing environment
• Direct experience managing or working closely with Contract Manufacturing Organizations (CMOs)

Strong understanding of:

• Design controls
• Process validation (IQ/OQ/PQ)
• FDA Quality System Regulations (21 CFR Part 820)
• ISO 13485
• CAPA and change control systems
• Experience collaborating with Quality, Regulatory, and R&D teams in a regulated environment

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.

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 [e-mail] 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.

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