Quality Control Technician - Thursday - Sunday 6:00AM to 4:00 PM

Southend Pharmacy; Houston (TX); On-site; USD 60,000 - 65,000; Full time

Benefits offered by this job

Full benefits package

Job summary

Southend Pharmacy in Houston, TX is seeking a Quality Control Technician to ensure safety and quality in the compounding sterile environment in a 503A pharmacy. The role involves routine inspections, environmental monitoring of cleanrooms, testing for sterility, endotoxin, potency, and documentation per USP <797> standards.

Onsite work is required with a Thu-Sun 6:00 AM–4:00 PM shift. Candidates need at least a high school diploma and 1–2 years QC experience; strong attention to detail and

Qualifications

• High school diploma or equivalent required.
• 1–2 years of quality control experience in hospital, pharmacy, sterile compounding, laboratory or related healthcare environment.
• Experience with USP <797> and USP <800>, cGMP principles, and state/federal pharmacy regulations.

Responsibilities

• Inspection/Walkthroughs of the cleanroom to ensure compliance before production.
• Environmental monitoring of cleanrooms and controlled areas for microbial contamination per USP <797>.
• Conduct quality tests on compounded sterile preparations (sterility, endotoxin, potency, pH).
• Maintain records of QC activities, test results and calibration logs.

Skills

Attention to detail

Documentation

Teamwork

Independent work

Education

High school diploma

Science degree preferred

Tools

Microsoft Office

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Quality Control Technician - Thursday - Sunday 6:00AM to 4:00 PM

Full-Time Technical Houston, TX, US

11 days ago Requisition ID: 1383

Salary Range: $60,000.00 To $65,000.00 Annually

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 compounding and transparent processes.

Job Summary

The Quality Control (QC) Technician will be responsible for but not limited to ensuring the safety and quality of the compounding sterile environment in a 503A pharmacy by performing routine inspections, environmental monitoring of the cleanroom and personnel monitoring, media promotion testing and reading of final results, notation of temperature/humidity/air pressure, conducting quality tests sample submissions (sterility, endotoxin, potency), occasionally writing and participating in investigations , and maintaining accurate documentation per USP <797> standards.

This is a full-time, onsite position located at Southend Pharmacy, 4802 North Sam Houston Pkwy W, Suite 100, Houston, TX 77086. Candidates must be able to work onsite as scheduled. Weekends may be required based on business needs.

Key Responsibilities

• Inspection/Walkthroughs
  • Perform routine walkthroughs of the cleanroom suite to ensure compliance before production.
• Perform routine environmental monitoring of cleanrooms and other controlled areas, including personnel, air and surface sampling for microbial contamination, to ensure compliance with USP <797> standards.
• Media promotion testing and reading of final results
• Daily notation of temperature, humidity, and air pressure of applicable sites and locations
• Quality Testing:
  • Conduct quality control tests on compounded sterile preparations, including sterility, endotoxin, potency, and pH testing, as applicable.
• Documentation and Compliance:
  • Maintain accurate and detailed records of QCactivities, including transfer dates, test results, environmental monitoring data, and equipment calibration logs, ensuring compliance with regulatory requirements.
• Equipment Maintenance:
  • Calibrate, clean, and maintain laboratory equipment used in QC testing incubators, a ir instruments, and analytical instruments.
• SOP Adherence:
  • Follow and enforce Standard Operating Procedures (SOPs) for compounding, testing, and cleaning processes to ensure consistency and compliance.
• Investigations and CAPA:
  • Assist in investigating out-of-specification (OOS) results, deviations, or non-conformances, and support the development and implementation of Corrective and Preventive Actions (CAPA).
• Training Support:
  • Assist in training pharmacy staff on proper aseptic techniques, gowning procedures, and compliance with USP <797> standards.
• Inventory Management:
  • Monitor and maintain inventory of QC testing supplies, reagents, and media, ensuring availability and proper storage conditions.
• Collaboration: Work closely with compliance, pharmacists, compounding technicians, and quality assurance (QA) staff to ensure seamless operations and adherence to

quality standards.

• Regulatory Preparedness:
  • Support preparation for inspections by state boards of pharmacy, FDA, or other regulatory bodies, ensuring all QC documentation and processes are audit-ready.

Qualifications

• High school diploma or equivalent required.
• Minimum of 1–2 years of quality control experience in a hospital, pharmacy, sterile compounding, laboratory, or other regulated healthcare environment.
• Experience with USP <797> and USP <800> guidelines, cGMP principles, and

state/federal pharmacy regulations.

• Strong attention to detail and ability to follow complex protocols.
• Excellent documentation and organizational skills.
• Ability to work independently and collaboratively in a team environment.
• Ability to work in a cleanroom environment with full PPE on for extended periods of time
• Strong communication skills, both written and verbal.
• Minimum of 2 years of experience with Microsoft Office (e.g., Excel, Word,

Google Sheets, GoogleDocs) for documentation and reporting.

Preferred

• Associate’s or Bachelor’s degree in a science-related field (e.g., biology,
• microbiology, chemistry).
• Experience in a sterile compounding pharmacy microbiology laboratory, or related field preferred.
• Certification as a Pharmacy Technician (CPhT) Texas preferred, or able to acquire trainee license immediately upon employment.
• Basic understanding of microbiology and analytical testing methods
• Experience in a 503A or 503B pharmacy quality control experience.
• Laboratory experience and Good Laboratory Practices (GLP).

Physical Requirements

• Ability to stand for extended periods, wear personal protective equipment (PPE), and work in a controlled cleanroom environment.

Shift Schedule:

• Day Shift - Thursday - Sunday
• Hours: 6:00 AM to 4:00 PM

What We Offer:

• Full benefits package including medical, vision, dental, 401(k) with company match, PTO, Flex days, holidays, and more!

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

Southend Pharmacy 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 & 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 immediate assistance or accommodations during the application or interview process, please contact us at [e-mail].

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 compounding and transparent processes.

Job Summary

The Quality Control (QC) Technician will be responsible for but not limited to ensuring the safety and quality of the compounding sterile environment in a 503A pharmacy by performing routine inspections, environmental monitoring of the cleanroom and personnel monitoring, media promotion testing and reading of final results, notation of temperature/humidity/air pressure, conducting quality tests sample submissions (sterility, endotoxin, potency), occasionally writing and participating in investigations , and maintaining accurate documentation per USP <797> standards.

This is a full-time, onsite position located at Southend Pharmacy, 4802 North Sam Houston Pkwy W, Suite 100, Houston, TX 77086. Candidates must be able to work onsite as scheduled. Weekends may be required based on business needs.

Key Responsibilities

• Inspection/Walkthroughs
  • Perform routine walkthroughs of the cleanroom suite to ensure compliance before production.
• Environmental Monitoring:
  • Perform routine environmental monitoring of cleanrooms and other controlled areas, including personnel, air and surface sampling for microbial contamination, to ensure compliance with USP <797> standards.
• Media promotion testing and reading of final results
• Daily notation of temperature, humidity, and air pressure of applicable sites and locations
• Quality Testing:
  • Conduct quality control tests on compounded sterile preparations, including sterility, endotoxin, potency, and pH testing, as applicable.
• Documentation and Compliance:
  • Maintain accurate and detailed records of QCactivities, including transfer dates, test results, environmental monitoring data, and equipment calibration logs, ensuring compliance with regulatory requirements.
• Equipment Maintenance:
  • Calibrate, clean, and maintain laboratory equipment used in QC testing incubators, a ir instruments, and analytical instruments.
• SOP Adherence:
  • Follow and enforce Standard Operating Procedures (SOPs) for compounding, testing, and cleaning processes to ensure consistency and compliance.
• Investigations and CAPA:
  • Assist in investigating out-of-specification (OOS) results, deviations, or non-conformances, and support the development and implementation of Corrective and Preventive Actions (CAPA).
• Training Support:
  • Assist in training pharmacy staff on proper aseptic techniques, gowning procedures, and compliance with USP <797> standards.
• Inventory Management:
  • Monitor and maintain inventory of QC testing supplies, reagents, and media, ensuring availability and proper storage conditions.
• Collaboration: Work closely with compliance, pharmacists, compounding technicians, and quality assurance (QA) staff to ensure seamless operations and adherence to

quality standards.

• Regulatory Preparedness:
  • Support preparation for inspections by state boards of pharmacy, FDA, or other regulatory bodies, ensuring all QC documentation and processes are audit-ready.

Qualifications

• High school diploma or equivalent required.
• Minimum of 1–2 years of quality control experience in a hospital, pharmacy, sterile compounding, laboratory, or other regulated healthcare environment.
• Experience with USP <797> and USP <800> guidelines, cGMP principles, and

state/federal pharmacy regulations.

• Strong attention to detail and ability to follow complex protocols.
• Excellent documentation and organizational skills.
• Ability to work independently and collaboratively in a team environment.
• Ability to work in a cleanroom environment with full PPE on for extended periods of time
• Strong communication skills, both written and verbal.
• Minimum of 2 years of experience with Microsoft Office (e.g., Excel, Word,

Google Sheets, GoogleDocs) for documentation and reporting.

Preferred

• Associate’s or Bachelor’s degree in a science-related field (e.g., biology,
• microbiology, chemistry).
• Experience in a sterile compounding pharmacy microbiology laboratory, or related field preferred.
• Certification as a Pharmacy Technician (CPhT) Texas preferred, or able to acquire trainee license immediately upon employment.
• Basic understanding of microbiology and analytical testing methods
• Experience in a 503A or 503B pharmacy quality control experience.
• Laboratory experience and Good Laboratory Practices (GLP).

Physical Requirements

• Ability to stand for extended periods, wear personal protective equipment (PPE), and work in a controlled cleanroom environment.

Shift Schedule:

• Day Shift - Thursday - Sunday
• Hours: 6:00 AM to 4:00 PM

What We Offer:

• Full benefits package including medical, vision, dental, 401(k) with company match, PTO, Flex days, holidays, and more!

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

Southend Pharmacy 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 & 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 immediate assistance or accommodations during the application or interview process, please contact us at [e-mail].

Shift Schedule:
Day Shift - Thursday - Sunday
Hours: 6:00 AM to 4:00 PM