Incoming Quality Control (IQC) Supervisor
Hims & Hers · New Albany, Ohio · US
Quality Improvement
On-site
Dentist
Demand70
Career growth62
Healthcare fit64
Remote potential15
5-year outlook
Supervisory QA/QC roles in regulated pharmaceutical compounding tend to offer stable compensation with progression toward quality management or site quality leadership. Exact pay is not stated and will depend on location, experience, and facility type.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-27
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United States
- Profession fit
- Dentist
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering for pharmacists or pharma-quality professionals with 503A/503B or cGMP QA/QC experience who want a supervisory industry role. Clinicians without regulated manufacturing or quality experience should not prioritize this posting.
Who should apply
Pharmacists with sterile compounding or 503A/503B quality experience, pharma QA/QC professionals seeking supervisory responsibility, and healthcare graduates with cGMP manufacturing or quality systems backgrounds.
CV angle
Frame real compounding pharmacy, sterile operations, documentation review, USP compliance, audit preparation, deviation/CAPA, supplier qualification, and team leadership experience. Emphasize regulated-environment QA/QC work and data integrity; do not claim manufacturing quality experience that was not actually performed.
Skills to highlight
- 503A/503B or cGMP quality systems
- Sterile compounding and USP compliance
- Incoming material release and disposition
- CoA/CoC and vendor documentation review
- Deviation, nonconformance, and OOS management
- Supplier qualification and audit support
- Team supervision and training
- Data integrity and risk assessment
Role summary
A supervisory quality role overseeing incoming raw material and component inspection, documentation review, release/disposition, supplier quality, deviations, audits, and continuous improvement within a 503A sterile compounding facility.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.