Quality Assurance Intern

Quality Control (QC) Intern

Location: Greenville, SC

Department: Quality Control

Duration: Summer 2026

Schedule: Full-time (40 hours/week)

Pay: $22-25/hour

Position Overview

PAI Pharma is seeking a motivated and scientifically curious QC Intern to support compendial method updates and analytical testing within the Quality Control laboratory.

This internship provides hands-on experience with laboratory instrumentation, analytical testing, and technical documentation. The selected candidate will contribute to method verification and improvement activities aligned with USP (United States Pharmacopeia) standards, gaining valuable exposure to regulatory-driven laboratory work.

Key Responsibilities

• Train on and utilize basic to intermediate laboratory instruments and techniques

• Perform analytical testing under supervision of QC leadership and senior analysts

• Follow all SOPs, cGMP requirements, and data integrity standards

• Accurately document test results and observations

• Assist in maintaining a compliant and organized laboratory environment

Key Projects

• Support USP compendial (cUSP) method verifications

• Assist in analytical method improvements and optimization efforts

• Contribute to technical writing, including protocols and reports

• Help ensure methods meet regulatory and quality standards

Learning Objectives

Through this internship, the selected candidate will:

• Gain hands-on experience with analytical instrumentation and lab techniques

• Learn how USP monograph updates impact laboratory testing

• Develop skills in method verification and continuous improvement

• Build experience in technical writing and scientific documentation

• Understand regulatory expectations within a pharmaceutical QC environment

Qualifications

• Currently pursuing a degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field

• Strong interest in analytical chemistry or laboratory sciences

• Attention to detail and ability to follow structured procedures

• Strong written and verbal communication skills

• Ability to work both independently and within a team

Preferred Qualifications

• Prior laboratory or academic research experience

• Familiarity with analytical techniques (HPLC, UV, etc.)

• Interest in pursuing a career in Quality Control or Analytical Development

What You’ll Gain

• Hands-on experience in analytical testing and method development

• Exposure to USP standards and regulatory requirements

• Opportunity to contribute to real lab method improvements

• Experience writing technical protocols and reports

• Mentorship from experienced QC scientists

Physical Requirements/Working Conditions:

To perform this job successfully, an individual must be able to perform the essential job functions satisfactorily. PAI is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, PAI will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer. PAI uses E-Verify.

PAI Pharma is a nicotine-free campus, meaning the use of nicotine products—including cigarettes, vaping, chewing tobacco, and any other nicotine-containing substances—is strictly prohibited on company property. All employees should be able to complete their full shift without the need to use nicotine. By joining PAI Pharma, you agree to adhere to our nicotine-free workplace policy, which supports a healthier environment for all employees.

EEO Employer / Veteran / Disabled