Quality Control Manager, Sterile
Hims & Hers · Mesa, Arizona · US
Posted 60+ days ago
Quality Improvement
On-site
Not yet analysed
Demand80
Career growth75
Healthcare fit72
Remote potential10
5-year outlook
Competitive for the pharmaceutical quality control sector, with potential for advancement into senior quality assurance or regulatory affairs roles. Salary growth is steady given the critical nature of sterile compounding compliance.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-08-26
Intelligence details
Why this is worth applying to
Pharmacists with sterile compounding or quality control experience should consider this role as a strong non-clinical career pivot into healthcare operations and compliance. It offers leadership opportunities and leverages clinical knowledge in a regulatory-focused setting.
Who should apply
Pharmacists with experience in 503A compounding, quality assurance, or regulatory compliance; allied health professionals with QC lab experience; healthcare graduates with strong science backgrounds and interest in pharmaceutical quality.
CV angle
Highlight any experience with USP standards, environmental monitoring, CAPA investigations, and batch record review. Emphasize leadership in quality assurance, attention to regulatory detail, and ability to collaborate with pharmacy and microbiology teams.
Skills to highlight
- Sterile compounding
- USP 797/795/800 compliance
- Environmental monitoring
- CAPA and root cause analysis
- Documentation and record control
- Team leadership
- Regulatory knowledge (FDA, state boards)
Role summary
The Quality Control Manager oversees all QC activities for sterile compounded preparations, ensuring compliance with USP, FDA, and state regulations. This includes product testing, environmental monitoring, deviation management, and documentation to maintain patient safety and quality standards.
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