<p>The intern will work closely with the Quality Assurance team to support day-to-day operations in a fast-paced distribution center environment. This role will involve assisting with various quality assurance tasks, including document control, metrics reporting, and process review.</p> <p>Key Responsibilities:</p> <ul> <li>Assist the Kentucky Quality Assurance team with day-to-day tasks, including but not limited to document control, monthly metrics reporting, and review processes for accuracy. </li><li>Identify areas for improvement from a quality assurance perspective and assist in developing solutions. </li><li>Support quality assurance with diverse projects, gaining exposure to regulatory compliance and CGMP standards in the pharmaceutical industry. </li><li>Collaborate with team members in a fast-paced office environment, balancing multiple tasks while maintaining attention to detail. </li><li>Develop strong communication skills through writing reports and presenting findings to the QA team. </li></ul> <p>Qualifications & Skills:</p> <ul> <li>Currently enrolled in a degree program in Biology, Chemistry, Physics, or a related field. </li><li>Working knowledge of Microsoft Word and Excel for documentation and data analysis. </li><li>Detail-oriented with the ability to multitask and manage time effectively. </li><li>Strong verbal and written communication skills, with the ability to convey information clearly and concisely. </li><li>Strong analytical and problem-solving skills, demonstrating the ability to identify issues and propose effective solutions. </li><li>Ability to work both independently and collaboratively in a team environment. </li></ul> <p>Why Join Us?</p> <ul> <li>Gain valuable experience in quality assurance within a pharmaceutical distribution center, learning about compliance with CGMP standards. </li><li>Develop practical skills in document control, metrics reporting, and quality process improvement. </li><li>Work alongside experienced professionals in a dynamic and fast-paced environment. </li><li>Contribute to projects that have a direct impact on the quality and compliance of pharmaceutical products. </li></ul>