Intern - GMP QA

Cayman ChemicalAnn Arbor, MI
15h

About The Position

Headquartered in Ann Arbor, Michigan, Cayman Chemical Company supplies scientists worldwide with the resources necessary for advancing human and animal health. We offer a vast product catalog that is constantly growing to meet the needs of our clients. Additionally, we provide service programs that include comprehensive solutions to drive clients’ projects to completion. Our mission is to make research possible. That starts by employing a talented and highly qualified group of experts that develop the tools to support research scientists. Currently, we are looking to add an Intern - GMP QA to the team:

Requirements

  • Enrolled in an accredited college/university pursuing a degree in a Science related field (e.g., Chemistry, Chemical Engineering, Biology, Materials Science, or related discipline).
  • An outstanding academic performer 3.0 / 4.0 GPA or equivalent academic requirement.
  • Interest in quality assurance, regulatory compliance, or manufacturing environments.
  • Proficiency with Microsoft Office applications (Word, Excel, Outlook, SharePoint).
  • Strong attention to detail and organizational skills, ability to work independently while collaborating effectively within a team.
  • Ability to follow written procedures and maintain data integrity.
  • Basic understanding of laboratory safety.
  • Available to work 5/11/26 through 8/7/26 .
  • Demonstrates Cayman’s Core Values – Integrity, Collaboration, People, Learning, and Excellence.

Responsibilities

  • Assist in drafting, organizing, and maintaining Drug Master File (DMF)–related documentation under QA guidance.
  • Support shipping and logistics compliance activities, including review, organization, and filing of shipping documentation and records.
  • Perform digital and physical document filing in compliance with document control and record retention requirements.
  • Assist with change management activities, including preparation, tracking, and documentation of change controls related to manufacturing, equipment, and processes.
  • Maintain accurate and organized records in accordance with GMP expectations.
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