Lead Pharmacist, Pharmacy Compliance

OpenLoop Health, Inc

$110K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • B.S. in Pharmacy or Pharm.D. from an ACPE-accredited institution with an active pharmacist license.
  • 3+ years in compounding pharmacy operations or pharmaceutical QA at a licensed 503A facility.
  • Hands-on experience with environmental monitoring programs and CAPA systems.
  • Practical command of USP standards relevant to compliance and operations.
  • Collaborative communicator, able to translate complex regulations into clear operational guidance.

Responsibilities

  • Own day-to-day compliance with USP standards and audit readiness.
  • Manage environmental monitoring and ensure adherence to quality standards.
  • Maintain and train staff on the SOP library and compliance procedures.
  • Run personnel training and competency assessments as per USP requirements.
  • Oversee the CAPA program and ensure closed-loop corrective actions.
  • Coordinate compliance related to engineering controls and risk assessments.
  • Conduct mock inspections and prepare for regulatory body interactions.

Benefits

  • Medical, Dental, and Vision plans
  • Flexible Spending/Health Savings Accounts
  • Flexible PTO
  • 401(k) + Company Match
  • Life Insurance and Pet insurance
Full Job Description
About the Role

California Quality Pharmacy is looking for a Lead Pharmacist, Pharmacy Compliance to serve as the on-site compliance authority at its licensed compounding facility - owning USP , , and program execution, maintaining inspection readiness, and acting as the primary compliance interface between the site and centralized pharmacy leadership. This role reports directly to the corporate compliance leadership team.

What You'll Do
  • Own day-to-day USP , , and (2023) compliance - keeping operations, controls, personnel practices, and quality systems current, documented, and audit-ready.
  • Manage the environmental monitoring program: viable air and surface sampling, non-viable particle and pressure/temperature/humidity tracking, action level investigation, and CAPA.
  • Maintain the SOP library - draft, update, version-control, and train personnel on all compliance-related procedures.
  • Run the personnel training and competency program per USP Section 7: initial and ongoing assessments, media fill, gloved fingertip sampling, garbing, and remediation.
  • Own the site CAPA program - deviation documentation, root cause analysis, corrective action tracking to verified closure, and trend reporting to leadership.
  • Maintain facility qualification records: ISO certification schedules, equipment re-qualification triggers, and calibration documentation.
  • Coordinate USP compliance: engineering controls, PPE protocols, Assessment of Risk, and spill response readiness.
  • Oversee MFR/CR completeness, BUD documentation, incoming material/COA review, and supplier qualification records.
  • Conduct mock inspections and gap assessments; support response to state board, FDA, or accreditation survey findings.
  • Manage product complaints, adverse event reporting, and site-level recall procedures.
  • Other duties as assigned.


Who You Are
  • B.S. in Pharmacy or Pharm.D. from an ACPE-accredited institution with an active, unrestricted pharmacist license in the state of practice.
  • Additional state pharmacist licensure is beneficial, but not required
  • 3+ years of hands-on experience in sterile compounding operations or pharmaceutical QA at a licensed 503A facility or 5+ years in pharmaceutical quality/compliance without direct 503A experience, with commitment to complete USP training in 90 days.
  • Practical command of USP , and (2023) - EM programs, competency requirements, and quality systems.
  • Experience with deviation investigations, CAPA, and environmental monitoring data analysis.
  • Disciplined documenter, risk-based thinker, and self-directed - able to manage competing compliance obligations without close oversight.
  • Collaborative communicator who can translate regulatory requirements into clear operational direction for staff and escalate clearly to leadership.


Required Qualifications
  • Active, unrestricted pharmacist license in the state of practice.
  • B.S. in Pharmacy or Pharm.D. from an ACPE-accredited institution.
  • 3+ years in compounding pharmacy operations or pharmaceutical QA at a licensed 503A facility.
  • Working knowledge of USP , and (2023).
  • Hands-on experience with EM programs, deviation management, or CAPA systems.


Preferred Qualifications
  • Experience at a state-licensed 503A sterile compounding pharmacy.
  • Familiarity with state board inspection processes and sterile compounding enforcement.
  • ISO 5/7/8 cleanroom classification and NABP/PCAB accreditation experience.
  • Experience responding to inspection observations, FDA Form 483s, or voluntary disclosures.
  • Familiarity with compounding regulatory landscape.


Our Benefits

In addition, for salaried positions you would also be eligible for:
  • Medical, Dental, and Vision plans
  • Flexible Spending/Health Savings Accounts
  • Flexible PTO
  • 401(k) + Company Match
  • Life Insurance, Pet insurance, and more


Join California Quality Pharmacy, a growing 503A sterile compounding pharmacy based in Stockton, California. We specialize in sterile pharmaceutical compounding, delivering high-quality, patient-specific medications with a strong commitment to regulatory compliance and clinical excellence. As we continue to expand, we're looking for dedicated professionals who take pride in precision and patient care.

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