Internship opportunity to develop an understanding of training administration in a regulated pharmaceutical manufacturing environment, including Good Manufacturing Practice (GMP) training record retention requirements and training system maintenance. Support the Training Department with data collection, documentation, and process support related to training records, Learning Management System (LMS) administration, and audit readiness. The intern will complete one focused project during the term of employment and deliver a presentation of outcomes to select Training and/or Quality stakeholders. Ability to complete a 13-week program (from May 18, 2026 to August 14, 2026) and commit to 40 hours per week onsite in Shirley, NY.
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Job Type
Full-time
Career Level
Intern
Number of Employees
251-500 employees