Quality Control Supervisor

hims & hers
United States
Workplace: OnsiteFull timeFunction: Quality & Regulatory (Non-Software)Experience: 3+ yearsEducation: bachelorsSkills: ["Attention to detail","Documentation","Communication","Time management","Organizational skills"]

Oversee in-process and final product inspections in a large-scale non-sterile compounding pharmacy, ensuring raw materials and finished products meet safety, efficacy, and regulatory requirements. Partner with the Quality Control Manager on deviations, non-conformances, and customer complaints; maintain audit readiness; and document quality metrics. Train and mentor quality control and production teams, verify equipment and calibration schedules, and help implement USP and applicable cGMP practices.

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FursaFursa
hims & hers
hims & hers
1 month ago

Quality Control Supervisor

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI
Last checked: 21 hours agoStatus: Live
Reposted: similar role first listed 6 months ago

Job Summary

Oversee in-process and final product inspections in a large-scale non-sterile compounding pharmacy, ensuring raw materials and finished products meet safety, efficacy, and regulatory requirements. Partner with the Quality Control Manager on deviations, non-conformances, and customer complaints; maintain audit readiness; and document quality metrics. Train and mentor quality control and production teams, verify equipment and calibration schedules, and help implement USP <795> and applicable cGMP practices.
Location: United States
Workplace: Onsite
Employment Type: Full time
Job Function: Quality & Regulatory (Non-Software)
Seniority: Manager level

Key Responsibilities

  • •Supervise and execute in-process and final product inspections across compounding process stages.
  • •Ensure raw material and product compliance through quality checks and documentation reviews.
  • •Support investigations for non-conformances, deviations, and customer complaints.
  • •Conduct and document equipment verifications and assist with calibration schedules (e.g., balances, pH meters).
  • •Help implement USP <795> and applicable cGMP practices, including internal audits and audit readiness.

Pay and Benefits

Perks:Paid LeaveHealth InsuranceDentalVisionParental LeaveEquity401k

Key Requirements

  • •Minimum 3 years of quality control or assurance experience, preferably in non-sterile compounding or pharmaceutical manufacturing.
  • •Strong understanding of USP <795> standards and cGMP practices.
  • •Associate's or Bachelor’s degree in Chemistry, Biology, Quality Management, or related field (preferred).
  • •Excellent attention to detail with strong documentation and communication skills.
  • •Proficiency in Microsoft Office (Word, Excel, Outlook); MRP/ERP experience is a plus.
Experience:3+ yearsPharmaceutical manufacturingNon-sterile compoundingRegulated environmentsCGMP
Education:Bachelor's in Chemistry, Biology, Quality Management, or a related field
Skills:Attention to detailDocumentationCommunicationTime managementOrganizational skills
Licenses:Pharmacy Technician
Tech Stack:Microsoft OfficeWordExcelOutlookMRPERPMRP/ERPBalancesPH meters

Company Brief

hims & hers
A telehealth and consumer wellness platform offering personalized care and products across sexual health, hair, mental health, dermatology, weight loss and primary care via digital consultations, prescriptions, and fulfillment.
Industry: HealthTech
Company Size: Enterprise (1,001+ employees)
Revenue: USD 1B+
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: San Francisco, United States
Founded: 2017
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