Quality Assurance Investigations Specialist

Hims & Hers; Mesa (AZ); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Competitive salary

Unlimited PTO

Health benefits

401k with employer match

Employee Stock Purchase Program (ESPP)

Job summary

Hims & Hers is seeking an experienced Quality Assurance Investigations Specialist for our Gilbert, AZ compounding pharmacy. You will lead investigations into quality events, perform root‑cause analyses, and ensure compliance with USP standards and FDA regulations.

You’ll collaborate with QA, QC, and production to drive CAPAs and maintain thorough documentation for regulatory inspections. Monitors will be in a 8–5pm M-F schedule on-site.

Qualifications

• Bachelor's degree preferred in science, quality or engineering or equivalent.
• 3+ years in quality, manufacturing, or regulated industry; degree may be substituted.
• Pharmacy Technician license or willingness to obtain one.
• Strong understanding of USP <795>, <797>, <800>, FDA 21 CFR Parts 210 & 211, and cGMP.
• Experience with investigations, deviation management, and escalation procedures.
• Excellent attention to detail, documentation, and organizational skills.
• Strong written and verbal communication and cross-functional collaboration.

Responsibilities

• Investigate customer complaints and quality events with pharmacists.
• Lead, document, and coordinate investigations of deviations, nonconformances, complaints, and OOS results.
• Perform structured root cause analyses to determine true causes.
• Ensure timely initiation and closure of investigations within quality system timelines.
• Collaborate with production, QC lab, and QA to gather evidence and assess impact.
• Prepare clear, compliant investigation reports for regulatory inspections.
• Support CAPA actions and track effectiveness.

Skills

Investigations

Root cause analysis

Cross-functional collaboration

Documentation practices

Time management

Communication skills

Problem solving

Education

Bachelor's degree in science/quality/engineering

3+ years quality/manufacturing/regulatory experience

Pharmacy Technician license or trainee

Tools

TrackWise

MasterControl

Google Workspace

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:

We are seeking an experienced Quality Assurance Investigations Specialist to join the Quality Unit at our compounding pharmacy in Gilbert, Arizona. In this role, you will lead and support investigations into quality-related events within our 503A compounding pharmacy operations. Reporting to the Quality Assurance Manager, you will partner closely with Quality Control (QC) and Quality Systems to ensure deviations, nonconformances, complaints, and other quality events are thoroughly investigated with rigorous root cause analysis and complete documentation.

You will ensure investigations are conducted in compliance with applicable regulatory requirements, including USP <795>, <797>, and <800>.

M-F 8-5pm

Key Responsibilities:

Event Investigation & Root Cause Analysis

• Investigate customer complaints and quality-related events, working closely with pharmacists to assess product quality events
• Lead, document, and coordinate investigations of deviations, nonconformances, complaints, OOS results, and other quality events.
• Perform structured root cause analyses to determine true causes.
• Ensure timely initiation, progress, and closure of investigations within defined quality system timelines.
• Collaborate with production, the QC laboratory, and QA to gather evidence and assess event impact.

Corrective and Preventive Actions (CAPA)

• Identify and recommend appropriate CAPAs to prevent recurrence of issues.
• Ensure CAPA actions are practical, risk-based, and aligned with regulatory and company standards.
• Track CAPA implementation and verify effectiveness.

Compliance & Documentation

• Prepare clear, accurate, and compliant investigation reports in accordance with internal SOPs and regulatory requirements.
• Maintain complete records to support regulatory inspections and internal audits.
• Escalate critical issues to Quality leadership in a timely manner.

Cross-Functional Collaboration

• Work closely with QA, QC, and Quality Systems to ensure consistent application of investigation procedures.
• Facilitate communication between operations, technical teams, and quality groups during investigations.
• Participate in site-level quality review boards and investigation review committees.

Continuous Improvement

• Identify trends across investigations and recommend systemic improvements.
• Support training of staff on deviation reporting, investigation practices, and documentation standards.
• Contribute to the enhancement of site procedures for deviation and OOS management.

Qualifications:

Education & Experience

• Bachelor's degree preferred in a relevant discipline (science, quality, or engineering-related field), or an equivalent combination of education and experience.
• 3+ years of related experience in quality, manufacturing, or a regulated industry may substitute for a degree.
• Pharmacy Technician or trainee license, or willingness to obtain one.

Knowledge & Skills

• Strong understanding of USP <795>, <797>, and <800> standards, FDA 21 CFR Parts 210 & 211, and cGMP; GDP and GLP experience preferred.
• Experience with investigations, deviation management, and escalation procedures.
• Excellent attention to detail, documentation practices, and organizational skills.
• Excellent written and verbal communication skills, including technical writing.
• Strong collaboration skills across multidisciplinary teams.
• Ability to manage multiple investigations under tight timelines.
• Proficiency in Google Workspace; proficiency with electronic quality systems (e.g., TrackWise, MasterControl) preferred.

Key Competencies

• Analytical and detail-oriented mindset.
• Strong problem-solving and decision-making abilities.
• Clear and professional communication.
• High sense of accountability and ownership.
• Ability to work independently and within cross-functional teams.

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.

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