Sterile Quality Control Manager — Elevate Patient Safety

Hims; Mesa (AZ); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Competitive salary

Equity compensation

Unlimited PTO

Health benefits

401k with match

ESPP

Job summary

Hims is looking for a QC Manager to lead the quality control program for sterile compounding, ensuring patient safety and regulatory compliance. You will oversee product testing, environmental monitoring, investigations, and documentation across the QC team.

The role requires a Bachelor’s in a related field and 3–5 years of QC experience in a regulated environment, with strong knowledge of USP guidelines and cGMP. Mesa, AZ-based position with competitive benefits.

Qualifications

• Bachelor’s degree in Pharmaceutical Sciences or related field.
• Minimum 3–5 years of QC experience in sterile compounding, pharma, or biotech.
• Strong knowledge of USP <795>, <797>, <800>, cGMP and state regulations.
• Experience with investigations, root-cause analysis, and CAPA processes.
• Ability to interpret analytical data and maintain rigorous documentation.

Responsibilities

• Oversee sampling, testing, and documentation of sterile drug products for sterility, endotoxin, potency, identity, and pH.
• Coordinate with third-party labs, review COAs, and investigate test abnormalities.
• Lead environmental monitoring and gowning/line clearance training.
• Manage deviations, OOS investigations, and CAPA programs.
• Maintain quality batch records and data integrity across QC records.
• Support audits, risk assessments, change controls, and SOP updates.

Skills

Pharmaceutical QC

Sterile compounding

Quality management

Regulatory compliance

Data interpretation

Education

Bachelor’s degree in Pharmaceutical Sciences

Tools

LIMS

Job description

Hims is looking for a QC Manager to lead the quality control program for sterile compounding, ensuring patient safety and regulatory compliance. You will oversee product testing, environmental monitoring, investigations, and documentation across the QC team.

The role requires a Bachelor’s in a related field and 3–5 years of QC experience in a regulated environment, with strong knowledge of USP guidelines and cGMP. Mesa, AZ-based position with competitive benefits.