Compounding Pharmacist

Location: Albuquerque, NMDepartment: Eden PharmacyReports To: Lab Manager & Pharmacist-in-Charge (PIC)Employment Type: Full-TimeAbout Eden PharmacyEden Pharmacy is a rapidly growing compounding pharmacy focused on delivering innovative, high-quality pharmaceutical solutions that improve patient outcomes. As we continue expanding our formulary and introducing new compounded therapies, we are seeking a highly skilled and forward-thinking Compounding Pharmacist to lead formulation development, quality oversight, and production coordination across sterile and non-sterile operations.This is an opportunity for someone who thrives in a fast-paced, innovation-driven environment and is passionate about advancing compounding practices through research, process improvement, and operational excellence.Position OverviewThe Compounding Pharmacist will play a critical role in the development, oversight, and optimization of Eden Pharmacy’s compounded formulations. This individual will be responsible for quality assurance and quality control (QA/QC) across sterile and non-sterile preparations, formulation research and development, production scheduling, and collaboration with third-party laboratories for analytical and stability testing.The ideal candidate has direct experience developing and scaling new compounded formulations, managing production workflows, and maintaining compliance with USP standards and regulatory requirements.Key ResponsibilitiesFormulation Research & DevelopmentLead the development and optimization of new sterile and non-sterile compounded formulationsConduct formulation research, ingredient compatibility assessments, and process validation activitiesCreate and maintain master formulation records, batch records, and compounding proceduresEvaluate excipients, active pharmaceutical ingredients (APIs), packaging, and delivery systems for new productsCollaborate with leadership to expand Eden Pharmacy’s formulary and introduce innovative compounded therapiesSupport pilot batches and scale-up activities for new formulationsQuality Assurance & Quality Control (QA/QC)Oversee QA/QC activities for all sterile and non-sterile preparationsEnsure compliance with USP , USP , USP , FDA guidance, and applicable state board regulationsReview and approve batch records, deviation investigations, and quality documentationMonitor environmental controls, sterility assurance processes, and production quality metricsImplement and maintain quality systems that support operational excellence and patient safetyParticipate in audits, inspections, CAPA management, and continuous quality improvement initiativesStability & Third-Party Testing Coordination Partner with external analytical laboratories and testing facilities to coordinate:Stability studiesSterility testingEndotoxin testingPotency testingBatch-specific analytical studiesReview and interpret laboratory reports and analytical dataMaintain documentation required for beyond-use dating (BUD) and formulation validationSupport formulation-specific data collection and regulatory documentation effortsProduction & Operational OversightDevelop and manage production calendars to ensure efficient workflow and inventory utilizationCoordinate compounding schedules based on prescription demand, inventory availability, and operational prioritiesCollaborate with pharmacy operations teams to optimize production throughput and minimize delaysSupport inventory forecasting for APIs, excipients, and packaging materialsIdentify operational bottlenecks and implement scalable production solutionsCross-Functional CollaborationWork closely with the Lab Manager, PIC, Pharmacy Operations, and leadership teamsSupport training and competency development for compounding staffAssist with SOP creation, workflow improvements, and implementation of new technologies or processesProvide subject matter expertise during product launches and operational scaling initiativesQualificationsRequired QualificationsActive Pharmacist license in good standingStrong understanding of USP , USP , and USP standardsExperience overseeing QA/QC processes in a compounding environmentExperience managing production schedules or production calendars in a pharmacy or manufacturing settingStrong documentation and analytical skillsAbility to work in a fast-paced, high-growth environmentPreferred QualificationsDirect experience with formulation research and development (R&D) for compounded medicationsExperience creating new formulations from concept through validation and productionExperience coordinating stability studies and third-party laboratory testingFamiliarity with batch record systems, formulation databases, and quality management systemsExperience scaling compounding operations or supporting formulary expansionMinimum 3–5 years of experience in sterile and/or non-sterile compounding pharmacy operationsBackground in process optimization or pharmaceutical manufacturing environmentsIdeal CandidateThe ideal candidate is highly detail-oriented, scientifically curious, operationally minded, and excited to help build and scale a modern compounding pharmacy. They are comfortable balancing innovation with compliance and can move seamlessly between formulation development, quality oversight, and production operations.They are proactive, collaborative, and energized by the opportunity to create new compounded therapies that meaningfully improve patient care.Why Join Eden PharmacyOpportunity to help shape and expand a rapidly growing formularyHigh-impact role with visibility across leadership and operationsCollaborative and innovative pharmacy environmentAbility to lead formulation development initiatives from the ground upCompetitive compensation and benefits packageMeaningful work focused on improving patient access and outcomes