Company Overview:

Strive Pharmacy is a personalized compounding pharmacy built on a simple conviction: medicine should fit the patient, not the other way around. We started Strive because we believed the pharmaceutical industry was overdue for a more human approach—one that prioritizes individualized care, clinical nuance, and genuine partnership with patients and providers.

Compounding gives us the tools to do that. Every formulation we prepare is built to the specific needs of a specific person, and every interaction we have is guided by that same commitment to personalized care.

We're growing, and we're looking for people who share that conviction. If you're ready to be part of a pharmacy that takes the work seriously and the people even more seriously, we'd like to meet you.

Mission:

Strive exists to disrupt an industry long overdue for a more personal approach to care. We put the human element at the center of everything: every formulation, every patient interaction, every provider partnership. We're not just a compounding pharmacy. We're a team on a mission to change what personalized healthcare looks and feels like.

Location: Tampa, Florida

Position Type: Full-Time

Schedule: Monday through Friday; 11:00 AM - 7:00 PM (weekends as needed)

Compensation Range: $140,000 - $155,000

Position Overview:

Strive Pharmacy is seeking a technical, quality-focused, and clinical leader for the role of Assistant Sterile Pharmacy Manager. Working alongside the Sterile Pharmacy Manager, this role provides operational leadership for the sterile compounding program, ensuring the highest standards of patient safety, product quality, sterility assurance, and regulatory compliance. The Assistant Sterile Pharmacy Manager oversees daily cleanroom operations, supports team development, verifies patient-specific prescriptions and batch documentation, and maintains compliance with sterile compounding standards across Strive’s 503A and 503B pharmacy operations.

Key Responsibilities

Leadership & Team Management: Provide direct supervision, workflow oversight, scheduling support, onboarding assistance, and competency evaluations for sterile compounding personnel while fostering a culture of quality, safety, and accountability.
Sterile Operations & Technical Oversight: Verify patient-specific prescriptions, master formulation records, and compounded lot documentation. Perform visual inspections, weight verification checks, and technical dosage calculations to ensure accuracy and compliance.
Cleanroom & Equipment Governance: Support cleanroom readiness, aseptic operating conditions, and equipment maintenance routines, including analytical balances, scales, and electronic measurement devices. Monitor chemical and pharmaceutical inventories for proper storage conditions, potency requirements, and expiration tracking.
Regulatory Compliance & Standards Enforcement: Ensure adherence to United States Pharmacopeia (USP) compounding standards, including USP <795>, USP <797>, and USP <800>, Current Good Manufacturing Practice (cGMP) regulations under 21 CFR Part 211, Food and Drug Administration (FDA) 503B guidance, and State Board of Pharmacy requirements.
Environmental Monitoring & Quality Assurance: Support environmental monitoring programs, cleanroom air quality testing, and microbiological surface sampling. Assist with root-cause investigations and development of Corrective and Preventive Action (CAPA) plans related to environmental or compounding deviations.
Staff Education & Competency Validation: Develop and deliver training programs for sterile compounding personnel focused on aseptic technique, garbing and gowning validation, hazardous drug handling, and regulatory compliance.Audit Readiness & Standard Operating Procedures (SOPs): Author, review, and maintain technical Standard Operating Procedures (SOPs). Support regulatory inspections and ensure operational documentation remains audit-ready.

Required Qualifications

Doctor of Pharmacy (PharmD) or Bachelor of Science in Pharmacy degree from an accredited pharmacy school