The Position
Join our Quality Assurance team as an intern and gain valuable experience in data management, documentation, and regulatory compliance. You will assist in organizing and maintaining records, improving system integration, and ensuring accurate documentation to support business operations. This role provides an opportunity to collaborate with cross-functional teams, enhance workflows, and contribute to regulatory readiness. Ideal for students looking to develop skills in quality management, compliance, and operational efficiency.
This is a 12-week, fully onsite Summer Internship Program paying $22.00/hr.
Responsibilities
- Assist in updating and maintaining vendor records in the Quality Management System (QMS) to improve system integration and data accuracy.
- Upload and organize vendor licenses, certificates, and agreements, ensuring proper tracking and accessibility.
- Support document management and compliance efforts, including linking records across systems for streamlined access.
- Assist in data consistency and quality control, ensuring accurate and up-to-date information across multiple platforms.
- Help prepare documentation for regulatory submissions and inspections, organizing and reviewing required materials.
Requirements:
- Currently enrolled student at an Accredited University or College and majoring in Life Sciences, Quality Assurance, Regulatory Affairs, or a related field
- Basic understanding of pharmaceutical quality systems (QMS) and regulatory compliance.
- Excellent verbal and written communication skills
- Ability to work independently while collaborating with Quality, Contracts, and Regulatory teams
- Strong problem-solving skills
- Eagerness to learn
