Quality Control Supervisor- Sterile (Nights)

New Albany, Ohiofull time

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Remote

mid

H1B: no

Hims and Hers Quality Control Supervisor-Sterile at Hims and Hers overseeing in-process and final product inspections in a sterile compounding pharmacy. Support compliance and mentor quality control staff during night shifts.

Responsibilities

We are seeking a detail-oriented and hands-on Quality Control Supervisor-Sterile to join our Quality team at our large-scale, sterile compounding pharmacy. Reporting to the Quality Control Manager, you will play a vital role in ensuring our products meet the highest standards of safety, efficacy, and regulatory compliance. This position is ideal for someone with a strong foundation in pharmaceutical or compounding environments who thrives on the production floor and is passionate about continuous quality improvement.
This position requires working onsite at our [New Albany, Ohio] facility & is a nights role.
Supervise and execute in-process and final product inspections across various stages of the compounding process.
Ensure raw material and product compliance through quality checks and documentation reviews.
Support the Quality Control Manager in investigations for non-conformances, deviations, and customer complaints.
Conduct and document equipment verifications and assist in calibration schedules (e.g., balances, pH meters).
Help implement and sustain compliance with USP and applicable cGMP practices.
Assist with internal audits, third-party inspections, and maintain audit readiness.
Maintain accurate records of inspections, results, and quality metrics for reporting purposes.
Train, coach, and mentor production and pharmacy team members on quality control procedures and standards.
Participate in drafting and revising SOPs, work instructions, and related documents.

Qualification

Excellent attention to detailProficiency in Microsoft Office (Word

Required

Minimum 3 years of experience in quality control or assurance, preferably in a sterile compounding or pharmaceutical manufacturing environment.
Strong understanding of USP standards and cGMP practices.
Associate's or Bachelor’s degree in Chemistry, Biology, Quality Management, or a related field (preferred).
Excellent attention to detail, with strong documentation and communication skills.
Proficiency in Microsoft Office (Word, Excel, Outlook); experience with MRP/ERP systems is a plus.
Experience in regulated environments (FDA 21 CFR 210/211 knowledge a plus).
Ability to manage multiple tasks simultaneously, with strong time management and organizational skills.
A Pharmacy Technician license or willingness to obtain one within the first six months of employment (we cover costs and will help you obtain your trainee hours).