Quality Assurance Technician (Mid-Shift)

Strive Pharmacy•San Antonio, TX

1d•$24 - $26•Onsite

About The Position

The Quality Assurance Technician ensures site-specific compliance in accordance with Strive Pharmacy’s Standard Operating Procedures (SOPs) and specifications. This role involves the quality review of documentation, label control, product inspections, and assisting with product release activities. Strive Pharmacy is dedicated to providing a better experience for each customer and clinic they work with, focusing on personalized medicine and a proactive approach to health. They aim to positively disrupt healthcare by emphasizing the human element in all interactions.

Requirements

Minimum of a High School Diploma or GED with relevant work experience.
Minimum of 2 years of experience in a quality or manufacturing department within a highly regulated industry (Pharmaceutical, Medical Device, or Allied Health Science preferred).
Proven experience reading, understanding, following, and reporting on Standard Operating Procedures.

Nice To Haves

Associate’s degree or higher in a technical or scientific discipline (Biology, Microbiology, Chemistry, or Pharmacy).
Experience in aseptic operations and familiarity with Pharmaceutical Quality Assurance practices.
Strong organizational skills, sharp attention to detail, and the ability to effectively troubleshoot issues.

Responsibilities

Perform product inspections for defects, leaks, and particulates.
Assist in media fill process validations, including the inspection of filled units.
Conduct environmental monitoring of personnel (as needed) and maintain accurate documentation.
Review compounding activities, including cleaning records, line clearance forms, inventory sheets, temperature logs, and Building Management System (BMS) alarms.
Ensure all documentation is complete.
Verify that raw materials meet specifications, account for labeling, and assist with raw material release and movement.
Document instances of non-compliance.
Under the direction of a supervisor, initiate quality events for deviation and non-compliant investigations, including routing samples to the appropriate lab for particulate or microbial analysis.
Maintain organized quality records (e.g., equipment calibration, maintenance files, training logs, cleanroom certifications, and Certificates of Analysis).
Support internal and external audits and actively participate in Quality Manager staff meetings.