Quality Control Technician - Morning (7:00 AM - 3:00 PM) at Southend Pharmacy – Houston, Texas

Company Overview

At Allia Health Group, the umbrella organization for Southend Pharmacy, Brello Health, and Woven, we don’t just follow industry trends—we redefine them. Our mission is to commoditize anti-aging solutions, making them affordable and accessible to the average consumer—not just the wealthy. By offering customized and cost-effective wellness products that follow cost-containment models, we aim to improve people’s quality of life and meet them wherever they are on their health journey.

About Southend Pharmacy

Southend 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 Summary

The Quality Control Technician will be responsible for ensuring the safety and quality of the sterile compounding environment in a 503A pharmacy by performing environmental monitoring, sample management, conducting quality testing, and maintaining accurate documentation in compliance with USP <797> standards. This role provides technical oversight while ensuring consistency in execution of environmental monitoring, documentation, and quality processes across shifts.

We are currently hiring for two full-time positions aligned to the same shift hours (7:00 AM - 3:00 PM) with different weekly schedules: Tuesday through Saturday, and Sunday through Thursday.

Key Responsibilities

• Identify potential quality risks in real time and initiate appropriate notifications or containment actions
• Ensure deviations, data integrity concerns, or incomplete documentation are identified promptly and escalated appropriately
• Ensure consistency in environmental monitoring practices, incubation handling, plate labeling, and documentation across shifts
• Participate in real-time coordination with Sterile leadership regarding sampling timing and cleanroom readiness
• Perform routine environmental monitoring of cleanrooms and controlled areas, including air and surface sampling for microbial contamination in compliance with USP <797>
• Conduct quality control testing on compounded sterile preparations, including sterility, endotoxin, potency, and pH testing
• Maintain accurate and detailed records of QC activities, including environmental monitoring data, test results, and calibration logs
• Calibrate, clean, and maintain laboratory equipment such as laminar airflow hoods, incubators, and analytical instruments
• Follow and enforce Standard Operating Procedures (SOPs) for compounding, testing, and cleaning processes
• Assist in investigations of deviations, OOS results, and non-conformances while supporting CAPA implementation
• Support training of pharmacy staff on aseptic technique, gowning, and USP <797> compliance
• Monitor and maintain inventory of QC supplies, reagents, and media
• Collaborate with pharmacists, compounding technicians, and QA teams to ensure quality alignment
• Support inspection readiness for regulatory bodies including FDA and state boards of pharmacy

What We Require

• High school diploma or equivalent
• Minimum of 1 year of experience in a sterile compounding pharmacy, microbiology lab, or related field
• Experience with USP <797> and USP <800> guidelines, cGMP principles, and pharmacy regulations
• Strong attention to detail and ability to follow complex protocols
• Experience in aseptic techniques and cleanroom operations
• Basic understanding of microbiology and analytical testing methods
• Strong documentation and organizational skills
• Ability to work both independently and collaboratively
• Strong written and verbal communication skills
• Minimum of 2 years of experience with Microsoft Office (Excel, Word, Google Sheets, Google Docs)

Preferred Requirement

• Prior experience in a QC or sterile operations role within a cleanroom environment
• Associate’s or Bachelor’s degree in a science-related field (biology, microbiology, chemistry)
• Experience in a 503A or 503B pharmacy environment
• Familiarity with Good Laboratory Practices (GLP)
• Experience supporting investigations, deviations, or regulatory inspections

What We Offer

• Pay: $60,000 – $65,000 per year (based on experience)
• Full benefits package including medical, dental, vision, and paid time off
• Supportive environment with opportunities for professional growth and training
• Full-time schedule

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

Allia Health Group 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 and 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 accommodations during the application process, please contact recruiting@alliahealth.co.