Research & Development Intern

The Research and Development Intern position is responsible for supporting formulation development, process optimization, and analytical testing within a 503B outsourcing facility. This role focuses on sterile compounded drug products under current Good Manufacturing Practices (cGMP) and regulatory guidelines established by the U.S. Food and Drug Administration. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.This internship runs through June 1 - July 31, 2026. Monday - Friday 8:00 AM - 4:00 PM at our Sugar Land, TX Location.What the R&D Intern Does Each Day:Assist in developing and optimizing formulationsConduct pre-formulation studies (pH, solubility, compatibility)Support scale-up activities from lab to pilot batchesDocument formulation protocols and experimental resultsPerform analytical testing (e.g., HPLC)Prepare samples and reagents following SOPsMaintain laboratory notebooks in compliance with cGMP standardsAssist in stability studies and data trackingObserve and assist with aseptic processing and sterile compoundingSupport environmental monitoring and cleanroom practicesHelp troubleshoot production or formulation issuesFollow cGMP and data integrity standardsAssist in deviation investigations and CAPA documentationEnsure proper documentation aligned with FDA 503B requirementsOther duties as assignedOur Most Successful R&D Interns:Are detail-oriented with strong verbal and written communications skillsMotivates others, shares knowledge, builds high performing team, shows respect towards others, gives constructive feedbackDisplay eagerness to learn and continuously improve, adapt quickly to change, and apply sound judgmentFoster team environment, invest in team members and peers by inclusion and listening, recognize employees effectively, demonstrate trustMinimum Requirements for this Role:High school diploma or GED from recognized institution or organization requiredMust be actively pursuing a bachelor's degree in Pharmaceutical Sciences; Chemistry; Chemical Engineering; Biomedial Engineering from an accredited institution with an anticipated graduation date within the next two yearsFamiliary with lab equipment and documentation practicesMust be in good standing with your accredited institution / universityMicrosoft Word and Excel skills18+ years of ageAble to successfully complete a drug and background checkMust be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visasAny of the Following Will Give You an Edge: Basic understanding of: cGMP regulations; Sterile Technique (preferred); Analytical Methods (HPLC)Benefits of Working at Quva:Set, full-time, consistent work scheduleNational, industry-leading high growth company with future career advancement opportunitiesAbout Quva:Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care.Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will."California Consumer Privacy Act (CCPA) Notice for Applicants and Employees Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Created: 2026-04-02