Research Compounding PharmacistSouthend 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.About the RoleSouthend's R&D / Formulations team is the engine behind our growing longevity and wellness portfolio — from GLP-1s and peptides to B12/glutathione injectables and a full range of non-sterile dosage forms. We're looking for a hands-on Research Compounding Pharmacist ready to develop formulations, build out clinical/regulatory documentation, and grow with a fast-scaling 503A pharmacy.This role partners closely with pharmacy operations, quality, regulatory, and leadership to design safe, compliant, and scalable formulations — spanning both sterile injectables and a wide range of non-sterile dosage forms (capsules, creams, gels, tablets, troches, rapid-dissolving tablets, and more). Current products include tirzepatide, semaglutide, B12, glutathione, and an expanding peptide line, with new products launching regularly.What You'll DoFormulation & Product DevelopmentDesign, develop, and optimize sterile and non-sterile formulations across a wide range of dosage formsSupport sterile compounding in the clean room (vialing, mixing) alongside sterile technicians and pharmacistsConduct formulation trials, stability studies, compatibility testing, and feasibility assessmentsHelp expand the product portfolio as new peptides and therapeutics come onlineClinical Documentation & Regulatory WritingCreate clear, clinically sound specification sheets covering common side effects, and contraindicationsDevelop well-referenced dosing protocols for new and existing products, with accurate, properly formatted citationsDraft and review SOPs and master formulation records (MFRs)Support regulatory submissions, internal audits, and inspections as neededRegulatory & ComplianceEnsure all R&D activities comply with USP <795>, <797>, and <800>, FDA guidance, and applicable state regulationsCross-Functional CollaborationPartner with operations to transfer formulations into productionWork with Quality Assurance on investigations, deviations, and CAPAs related to formulationsProvide technical guidance and training to pharmacists and techniciansContinuous ImprovementIdentify opportunities to improve product quality, efficiency, and scalabilityEvaluate new ingredients, technologies, and equipmentContribute to strategic planning for the product pipelineWhat We're Looking ForRequiredPharmD, BS in Pharmacy, or foreign pharmacy degree with an active Texas pharmacist license2–5 years of hands-on experience in compounding pharmacy, formulation development, or pharmaceutical R&D — ideally at a 503A or 503B pharmacyComfortable with hands-on lab work (compounding, vialing) — this is not a supervisory or PIC-level roleStrong written communication skills: able to produce accurate, regulatory-compliant, well-cited clinical documentsWorking knowledge of USP <795>, <797>, and <800>Willingness to relocate to the Houston area for this onsite rolePreferredSterile compounding experience strongly preferred; non-sterile experience highly valued (ideally both)Clinical experience developing dosing protocolsPublished work or strong scientific/technical writing backgroundBoard Certification in Sterile Compounding (BCSCP) or equivalentExperience with peptides, hormones, injectables, or complex dosage formsFamiliarity with pharmacy management or compounding software (training provided)BenefitsFull benefits package including medical, vision, dental, 401(k) with company match, PTO, flex days, holidays, and more!Southend Pharmacy is unable to offer visa sponsorship at this time. Candidates must be legally authorized to work in the United States without current or future sponsorship.Equal Opportunity Employer StatementSouthend Pharmacy is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.If you have any questions or require accommodations during the application process, please contact hours 8-5