Research & Development Intern

Quva • Sugar Land, TX

7h • Onsite

About The Position

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.

Requirements

• High school diploma or GED from recognized institution or organization required
• Must 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 years
• Familiary with lab equipment and documentation practices
• 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

• Basic understanding of: cGMP regulations; Sterile Technique (preferred); Analytical Methods (HPLC)

Responsibilities

• Assist in developing and optimizing formulations
• Conduct pre-formulation studies (pH, solubility, compatibility)
• Support scale-up activities from lab to pilot batches
• Document formulation protocols and experimental results
• Perform analytical testing (e.g., HPLC)
• Prepare samples and reagents following SOPs
• Maintain laboratory notebooks in compliance with cGMP standards
• Assist in stability studies and data tracking
• Observe and assist with aseptic processing and sterile compounding
• Support environmental monitoring and cleanroom practices
• Help troubleshoot production or formulation issues
• Follow cGMP and data integrity standards
• Assist in deviation investigations and CAPA documentation
• Ensure proper documentation aligned with FDA 503B requirements
• Other duties as assigned

Benefits

• Set, full-time, consistent work schedule
• National, industry-leading high growth company with future career advancement opportunities

What This Job Offers

• Job Type: Full-time
• Career Level: Intern
• Education Level: High school or GED
• Number of Employees: 251-500 employees