Non-Sterile Compounding Technician

Remedy•Houston, TX

About The Position

As a Non-Sterile Compounding Pharmacy Technician at Thirty Madison, now part of Remedy, you will prepare compounded non-sterile medications under the direct supervision of a licensed pharmacist. Work must comply with USP <795>, applicable USP <800> requirements, state Board of Pharmacy regulations, and facility standard operating procedures. The role supports growing production volumes across a range of pharmaceutical dosage forms and offers the opportunity to work with technologies such as 3D printing and tablet compression. You will prepare solid oral dosage forms, semi-solids, and oral liquids; operate specialized compounding and manufacturing equipment; perform in-process quality checks; and maintain accurate production, inventory, equipment, and cleaning documentation. You will help maintain a clean, compliant production environment and support quality assurance, audits, regulatory inspections, and continuous improvement initiatives.

Requirements

  • Active pharmacy technician license or registration in Texas, in good standing.
  • At least 2 years of pharmacy technician experience.
  • Working knowledge of USP <795> and applicable USP <800> requirements.
  • Experience preparing non-sterile pharmaceutical formulations, including solid oral dosage forms, semi-solids, or oral liquids.
  • Familiarity with pharmaceutical compounding equipment, including balances, mixers, capsule fillers, or tablet production equipment.
  • Strong pharmaceutical calculation skills and attention to detail.
  • Ability to accurately follow master formulation records, equipment operating instructions, and written SOPs without deviation.
  • Strong organizational skills and ability to maintain accurate production and quality documentation.
  • Ability to work efficiently in a production-focused environment while maintaining strict quality and safety standards.
  • Ability to safely operate compounding, mixing, tablet compression, and pharmaceutical production equipment.
  • Ability to follow applicable hygiene, gowning, and safety requirements.
  • Must pass fit-testing for respiratory protection where applicable.

Nice To Haves

  • PTCB Certified Pharmacy Technician (CPhT).
  • Experience in non-sterile compounding, pharmaceutical production, or a 503A/503B pharmacy environment.
  • Experience operating tablet presses, including Korsch equipment, or other pharmaceutical compression machinery.
  • Familiarity with pharmaceutical 3D printing, hot-melt extrusion (HME), or other advanced drug manufacturing technologies.
  • Experience with LMX mixers, powder blending, capsule filling, or semi-solid compounding.
  • Experience in a 503A compounding pharmacy or FDA-registered 503B outsourcing facility.
  • Experience handling hazardous or potent APIs under USP <800> containment requirements.
  • Familiarity with pharmaceutical quality testing, electronic batch records, and pharmacy management systems.
  • Knowledge of cGMP principles and pharmaceutical manufacturing practices.
  • Interest in professional development and potential cross-training in sterile compounding techniques.

Responsibilities

  • Prepare non-sterile compounded medications from approved master formulation records, including compressed tablets, capsules, 3D-printed tablets, creams, ointments, gels, transdermals, suspensions, and solutions.
  • Weigh, measure, mix, blend, and compound active pharmaceutical ingredients and excipients according to approved formulations and standard operating procedures.
  • Support preparation of patient-specific medication strengths and release profiles using pharmaceutical compounding technologies.
  • Operate 3D-printing and hot-melt extrusion equipment, including loading and calibrating the extruder, monitoring operating parameters, and producing tablets using approved print files.
  • Perform in-process quality checks on 3D-printed tablets, including weight, dimensions, and visual appearance.
  • Set up, operate, and clean Korsch tablet presses, including tooling changes and adjustments to compression force, fill depth, and turret speed.
  • Conduct tablet production quality checks, including weight, hardness, thickness, and friability testing.
  • Operate LMX mixers to prepare powder blends and semi-solid formulations using validated mixing processes.
  • Use supporting compounding equipment, including analytical balances, capsule fillers, ointment mills, and powder containment hoods or ventilated balance enclosures.
  • Verify ingredient quantities, NDCs where applicable, lot numbers, and expiration dates before compounding.
  • Stage and label compounded preparations for pharmacist verification and ensure documented final review before release.
  • Assign beyond-use dates according to approved formulation records and applicable USP standards.
  • Support batch production runs, including in-process checks, yield reconciliation, and production documentation.
  • Maintain a clean, organized, and compliant non-sterile compounding environment in accordance with applicable standards, regulations, and procedures.
  • Perform and document routine cleaning and maintenance of compounding equipment, production areas, and work surfaces.
  • Follow procedures to prevent cross-contamination and safely handle pharmaceutical ingredients, including hazardous or potent APIs when applicable.
  • Perform equipment calibration checks and document equipment readiness before production.
  • Follow safety procedures for powder handling, material transfers, and equipment cleaning, using appropriate engineering controls, containment equipment, and PPE.
  • Promptly report deviations, near misses, equipment malfunctions, and out-of-specification results.
  • Support internal audits, quality assurance activities, and regulatory inspections as directed.
  • Accurately and contemporaneously complete compounding records, batch production documentation, equipment logs, and cleaning records.
  • Maintain inventory of APIs, excipients, containers, packaging materials, and compounding consumables; rotate stock and monitor expiration dates.
  • Document ingredient usage, lot numbers, equipment settings, and in-process quality checks according to established procedures.
  • Assist with recall response, quarantine of suspect materials, and destruction documentation.
  • Support continuous improvement initiatives to enhance production efficiency, quality, and compliance.

Benefits

  • Medical, dental, and vision plan options described as robust and affordable.
  • Vacation time off policy with up to 10 vacation days accrued in the first year; accrual begins immediately.
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