Sterile Pharmacist – Precision Compounding & Patient Care

Southend Pharmacy

Houston (TX)

On-site

USD 120,000 - 150,000

Full time

4 days ago
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Benefits offered by this job

Medical benefits
Vision and dental benefits
401(k) with company match
PTO and holidays

Job summary

Southend Pharmacy in Houston seeks a Sterile Pharmacist to lead sterile compounding and distribution, working closely with technicians to ensure safe, accurate medication preparation. This role emphasizes adherence to USP <797> and regulatory standards, impacting patient care across diverse populations.

Texas licensure and at least one year of sterile pharmacy experience are required, with opportunities to contribute to process improvements and new formulations in a modern 503A setting.

Qualifications

  • Bachelor's degree in pharmacy or related field as listed.
  • Active, unrestricted Pharmacist License (TX State Board).
  • Minimum of one year of sterile pharmacy experience.
  • Expert proficiency in USP <797> sterile compounding standards and related cGMP regulations.
  • Strong attention to detail, problem-solving, and communication within a team.

Responsibilities

  • Compound prescriptions with precision following USP <797> standards.
  • Verify accuracy of prescriptions and ensure proper distribution.
  • Collaborate with technicians to manage sterile compounding workflow and records.
  • Oversee inventory and replenish sterile product supplies.
  • Engage in research to improve compounding techniques and formulations.

Skills

Attention to detail
Problem-solving
Communication skills

Education

Bachelor's degree in Pharmacy
Pharm.D. (preferred)

Job description

Southend Pharmacy in Houston seeks a Sterile Pharmacist to lead sterile compounding and distribution, working closely with technicians to ensure safe, accurate medication preparation. This role emphasizes adherence to USP <797> and regulatory standards, impacting patient care across diverse populations.

Texas licensure and at least one year of sterile pharmacy experience are required, with opportunities to contribute to process improvements and new formulations in a modern 503A setting.

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