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The Pharmacy Hub

Tech-enabled compounding and prescription fulfillment

Head of Sterile Compounding

Bioprocess & Biomanufacturing +1Updated on Nov 15
Full-timeFort Lauderdale, FL, USA$185k - $225k

About the Job

Requirements

  • PharmD or Bachelor of Science in Pharmacy.
  • Hold an active pharmacist license in good standing and be able to obtain Florida pharmacist licensure as required.
  • Have at least 10 years of progressive experience in sterile compounding, pharmacy operations, quality, compliance, and team leadership.
  • Demonstrate experience building or substantially expanding a sterile compounding program.
  • Have extensive knowledge of USP <797> and USP <800>.
  • Have strong quality-system, cleanroom, and regulatory-inspection experience.
  • Have experience managing pharmacists and pharmacy technicians.
  • Understand aseptic processing, environmental monitoring, and contamination-control principles.
  • Have experience developing standard operating procedures, managing CAPA and deviations, and scaling process improvements.
  • Be able to stand, walk, and move through cleanroom and production environments for extended periods, including gowning or garbing as required.
  • Have high attention to detail, analytical and root-cause problem-solving skills, and the ability to lead cross-functional teams through complex, fast-changing priorities.

Responsibilities

  • Develop the sterile compounding program from initial design through operational readiness and sustained commercial operations, including the operating model, organizational structure, staffing plan, training program, and quality infrastructure needed to scale.
  • Build and mentor a high-performing team of pharmacists, technicians, quality personnel, and production leaders, embedding quality, safety, and accountability into daily operations.
  • Serve as the internal subject-matter expert on USP <797>, USP <800>, Florida Board of Pharmacy sterile-compounding requirements, and applicable DEA and FDA requirements, translating regulations into executable workflows for frontline staff.
  • Develop and oversee the pharmaceutical quality system, including deviations, CAPA, change control, investigations, environmental monitoring, and vendor and equipment qualification.
  • Partner with Engineering, Facilities, architects, and contractors on cleanroom design, construction, qualification, and ongoing maintenance, applying working knowledge of ISO-classified environments, airflow, HEPA filtration, and contamination control.
  • Design sterile production workflows that scale safely, and establish KPIs and dashboards for batch success rate, right-first-time percentage, yield, cycle time, and other production and quality metrics.
  • Partner with formulation scientists, analytical scientists, and R&D on injectable, ophthalmic, and other sterile formulations from initial development through robust, reproducible, scalable processes.
  • Build sterile training programs, develop trainers, create competency assessments, and coach team members into future supervisors and managers while remaining visible on the production floor.
  • Maintain continuous inspection readiness and lead preparation for Board of Pharmacy, FDA, and accreditation inspections and audits.
  • Partner with Technology and Operations to build sterile workflows into the company's ERP and pharmacy systems, including electronic batch records, barcode verification, and quality dashboards.

Desired Qualifications

  • Experience as a Director of Sterile Compounding, VP of Pharmacy Operations, Director of Quality, Director of Pharmacy, or Sterile PIC.
  • Experience in a 503A sterile compounding and/or 503B outsourcing facility.
  • Experience in cGMP manufacturing or hospital IV-room leadership.
  • FDA and/or Board of Pharmacy inspection experience.
  • Facility construction or cleanroom expansion experience.
  • Process validation, cleaning validation, and equipment qualification experience.
  • Formulation development, technology transfer, and commercial scale-up experience.
  • Experience implementing automation or digital quality systems.

About the Company

The Pharmacy Hub

Tech-enabled compounding and prescription fulfillment

The Pharmacy Hub provides turnkey prescription fulfillment services for telehealth companies, clinics, digital health platforms, and pharmaceutical brands across the United States as a 503A compounding pharmacy and fulfillment center. It operates a fulfillment-as-a-service platform using proprietary software and automation to handle high-volume, non-sterile compounding in USP 795/800 cleanrooms, refrigerated shipping, and direct-to-consumer delivery, with white-label packaging and API integrations for seamless brand-preserving operations. It differentiates itself through a flat-fee model, high-volume scalability (up to 15,000 prescriptions per day), white-label capabilities, and LegitScript regulatory certification, serving clients from startups to hospitals and insurers. Its goal is to reduce clients' costs and accelerate speed-to-market by providing a scalable, compliant, and brand-preserving pharmacy solution.

Company size
11-50
Company stage
Not listed
Total funding
Not listed
Headquarters
Orlando, FL
Founded
2022

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