Job Title

Company OverviewSouthend Pharmacy is a modern 503A compounding pharmacy built on clinical precision, operational clarity, and a human-first approach. Licensed in 35+ states and focused on longevity-aligned therapeutics, we support providers and their patients with precision in compounding and transparent processes. Southend Pharmacy operates at the intersection of innovation, ambition, and clinical excellence-blending precision, clarity, and compassionate support to help providers deliver patient-centered, clinically guided care across every step of the treatment journey.Job SummarySouthend Pharmacy is seeking a dedicated Clinical Pharmacist - Sterile Compounding. This person will be responsible for the clinical oversight, preparation, and quality assurance of compounded sterile preparations (CSPs) in compliance with USP and standards. This role integrates clinical pharmacy knowledge with expertise in aseptic technique to ensure the safe and effective delivery of sterile medications. The pharmacist plays a key role in sterile production processes, quality assurance, regulatory compliance, and staff training.Key ResponsibilitiesClinical and Patient-Centered ResponsibilitiesInterpret and validate prescriber orders for sterile compounded medications, ensuring clinical appropriateness, dosing accuracy, and therapeutic suitabilityProvide clinical input on product selection, compounding alternatives, stability, and compatibility of medicationsEvaluate and monitor patient-specific data, including labs, to support optimal therapy outcomesCollaborate with prescribers and healthcare teams on individualized compounded therapies (e.g., parenteral nutrition, chemotherapy, ophthalmic solutions)Sterile Compounding OversightOversee or perform sterile compounding procedures in ISO-classified cleanrooms per USP and Ensure adherence to aseptic technique and proper gowning, workflow practices, and environmental controlsValidate compounding processes, including calculations, batch records, beyond-use dating (BUD), and labelingConduct final verification and release of compounded sterile preparations for dispensingRegulatory Compliance and DocumentationEnsure continuous compliance with federal and state regulations, including FDA guidelines, USP chapters, and Board of Pharmacy requirementsMaintain complete and accurate compounding documentation, including master formulation records, compounding logs, and cleaning schedulesParticipate in internal and external audits, inspections, and risk assessmentsImplement and uphold policies related to hazardous drug handling (USP ) and safe disposalQuality Assurance and ImprovementParticipate in cleanroom quality control activities, including air sampling, surface testing, and media fill testingInvestigate and document deviations, errors, and out-of-specification eventsSupport continuous quality improvement initiatives and adherence to pharmacy standard operating procedures (SOPs)Assist with environmental monitoring program evaluations and improvementsTraining and DevelopmentTrain and assess pharmacy staff (including technicians) on sterile compounding procedures, gowning, and aseptic techniqueEnsure ongoing staff competency, including periodic testing and continuing education complianceEducate healthcare providers on CSPs, storage conditions, and administration techniquesOperational SupportCollaborate with pharmacy leadership on workflow management, resource allocation, and inventory control of sterile supplies and APIsParticipate in the development and validation of new CSP formulations and processesMonitor and manage inventory for hazardous and sterile compounding ingredients to ensure availability and complianceWhat We OfferRequiredDoctor of Pharmacy (Pharm.D.) or BS of Pharmacy from an ACPE-accredited school of pharmacyLicensure & Certification:Active, unrestricted pharmacist license in the state of TexasSterile compounding and aseptic technique training (ACPE-accredited or equivalent)Hazardous drug handling certification (USP ) - may be obtained upon hireExperience:Minimum 1-3 years of experience in sterile compounding in a hospital, infusion center, or compounding pharmacyDemonstrated knowledge of USP , , and guidelinesExperience in handling cytotoxic and hazardous drugs preferredPreferredDeep understanding of sterile compounding techniques, cleanroom standards, and environmental monitoringAdvanced knowledge of drug stability, compatibility, and clinical pharmacologyStrong attention to detail, accuracy, and compliance with documentation standardsProficient in pharmacy information systems, sterile compounding software, and EMRsExcellent communication, collaboration, and problem-solving abilitiesAbility to work effectively under pressure and manage shifting prioritiesBoard Certification in Pharmacotherapy (BCPS) or Oncology Pharmacy (BCOP) preferredBenefitsFull benefits package including medical, vision, dental, 401(k) with company match, PTO, Flex days, holidays, and more!Southend Pharmacy does not provide employment visa sponsorship now or in the future. Applicants must be legally authorized to work in the United States without the need for current or future sponsorship.Equal Opportunity Employer Statement Southend Pharmacy is proud to be an Equal Opportunity Employer where we are committed to fostering a diverse and inclusive workplace. We are committed to cultivating a culture where all team members feel valued & respected. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetic information, disability, age, veteran status, or any other characteristics protected by applicable law. If you have any questions or require immediate assistance or accommodations during the application or interview process, please contact us at .10:30am to 7pm