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Quality Control Supervisor- Sterile (Nights)

Hims & Hers · New Albany, Ohio · US

Quality Improvement
On-site
Pharmacist
Dentist
Demand72
Career growth66
Healthcare fit78
Remote potential–
5-year outlook
Likely stable to modestly growing as sterile compounding and pharmaceutical QC experience accrues; supervisory experience can ladder into QC/QA management, though compensation will depend on market, shift premium, and licensure.
Clinical license
Required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-27

Intelligence details

Flexible work details

Engagement type
Permanent
Hours
Full-time
Eligible countries
United States
License jurisdiction
US
Profession fit
Pharmacist, 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 pharmacy or healthcare professionals with sterile compounding, quality, or regulated-environment exposure who want a non-patient-care compliance track. Less attractive if you cannot work nights onsite or do not meet the 3-year QC/QA experience bar.

Who should apply

Pharmacists, pharmacy technicians, healthcare graduates with compounding or laboratory quality exposure, and pharma/QC professionals interested in sterile compounding compliance and supervisory growth.

CV angle

Frame real pharmacy or compounding experience around medication safety, sterile technique, USP/cGMP awareness, documentation accuracy, deviation/non-conformance support, audit readiness, SOP adherence, equipment checks, and training or mentoring of colleagues.

Skills to highlight

  • Sterile compounding
  • Quality control inspections
  • cGMP and USP standards
  • Deviation and non-conformance documentation
  • SOP and work instruction support
  • Audit readiness
  • Equipment verification and calibration
  • Training and mentoring

Role summary

Supervise and perform quality control activities in a large-scale sterile compounding pharmacy, including in-process and final product inspections, documentation, deviation investigations, equipment verification, audit support, SOP revisions, and staff mentoring on night shift.

We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.