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hims & hers

Connects patients to online medical care

Quality Control Supervisor-Sterile

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeNew Albany, OH, USA

About the Job

Requirements

  • At least 3 years of experience in quality control or quality assurance; sterile compounding or pharmaceutical manufacturing experience is preferred.
  • Strong understanding of USP <797> standards and current good manufacturing practices.
  • Preferred associate's or bachelor's degree in Chemistry, Biology, Quality Management, or a related field.
  • Strong attention to detail and documentation skills.
  • Proficiency in Microsoft Office, including Word, Excel, and Outlook.
  • Experience in regulated environments; knowledge of FDA 21 CFR 210/211 is a plus.
  • Ability to manage multiple tasks simultaneously, with time-management and organizational skills.
  • A Pharmacy Technician license, or willingness to obtain one within the first six months of employment.
  • Ability to wear required personal protective equipment while handling hazardous drugs, including gloves, respiratory protection, and gowns.
  • Medical approval to wear respiratory protection, including negative- or positive-pressure respirators, N95, full-face respirator, SCBA, or PAPR.
  • Ability to meet the physical requirements, including walking up to 50% of the time, standing up to 100%, squatting and bending up to 20%, and lifting up to 80% during shifts of up to 12 hours; must be able to lift up to 50 pounds.
  • Willingness to confirm understanding of the potential teratogenic, carcinogenic, and reproductive risks of handling hazardous drugs.

Responsibilities

  • Supervise and perform in-process and final product inspections across stages of the compounding process.
  • Ensure raw materials and products comply with quality requirements through checks and documentation reviews.
  • Support the Quality Control Manager with investigations into non-conformances, deviations, and customer complaints.
  • Conduct and document equipment verifications and assist with calibration schedules for equipment such as balances and pH meters.
  • Help implement and maintain compliance with USP <797> and applicable current good manufacturing practices.
  • Assist with internal audits and third-party inspections, and maintain audit readiness.
  • Maintain accurate inspection, results, and quality-metric records for reporting.
  • Train, coach, and mentor production and pharmacy team members on quality-control procedures and standards.
  • Participate in drafting and revising standard operating procedures, work instructions, and related documents.

Desired Qualifications

  • Experience in a sterile compounding or pharmaceutical manufacturing environment.
  • Experience with MRP/ERP systems.
  • Knowledge of FDA 21 CFR 210/211.

About the Company

hims & hers

Connects patients to online medical care

Hims & Hers operates a consumer health platform that connects people with licensed providers for online consultations and ongoing care. Its Hims and Hers brands give customers access to services for hair loss, sexual health, mental health, skin care, and weight management, alongside prescription and nonprescription products. Providers assess patients and make treatment decisions, while the group coordinates digital records, follow-up, and fulfillment through owned and partner pharmacies. Revenue comes from product sales and subscriptions that combine recurring shipments with access to care. Hims & Hers was founded in 2017 and is headquartered in San Francisco, California.

Company size
1,001-5,000
Company stage
Post IPO Equity
Headquarters
San Francisco, California
Founded
2017

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