Sterility Assurance Intern

Quva•Sugar Land, TX

11d•Onsite

About The Position

The Sterility Assurance (SA) Intern is a direct labor role that will be exposed to gown qualification, EM/PM, media fills, SA investigations, and clean room monitoring. The person is dedicated to ensuring good aseptic practices and ensures units are collected, documented, and tested appropriately. The SA Intern also assists in monitoring the compounding activities to assess aseptic behavior in the clean room and provide feedback if concerns are found. This internship runs through June 1 - July 31, 2026. Monday - Friday 8:00 AM - 4:00 PM at our Sugar Land, TX Location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws

Requirements

High school diploma or GED from recognized institution or organization required
Must be actively pursuing a bachelor's degree from an accredited institution, with an anticipated graduation date within the next two years
Must be in good standing with your accredited institution / university
Microsoft Word and Excel skills
18+ years of age
Able to successfully complete a drug and background check
Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas

Nice To Haves

Drive achievement, expresses energy, shows accountability, ability to multi-task and work in a fast-paced, quality-rich environment
Demonstrated core values, professionalism, maturity through various campus or community sports, volunteer activities, or previous work history
Works closely with the department supervisor to ensure alignment on day-to-day priorities
Detail-oriented with strong verbal and written communications skills
Supports the development of a climate of quality and safety within the teams, by identifying and monitoring quality and safety standards

Responsibilities

Ensures company compliance to QuVa Pharma’s Standard Operating Procedures (SOPs) and Quality Management System (QMS)
Schedule & Shadow Media Fills
Observes technicians in compounding and routine clean room activities
Performs reading of media aseptic process simulations and Environmental/Personnel Monitoring (EM/PM) plates and accounting of all units
Maintains EM/PM records
Follows all regulatory guidelines, cGMP guidelines, and aseptic techniques as required by the job function
Assists in Sterility Assurance oversight where the business is responsible for adhering to current Good Manufacturing Practices (cGMPs) and provides feedback
Ensures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMP