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. Essential Duties and Responsibilities Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Support training record retention projects, ensuring compliance for electronic and GMP paper records (e.g., organization, reconciliation, scanning/filing support, controlled storage practices). Assist in ongoing maintenance of the Training Management System, including routine system auditing (e.g., training assignment checks, completion/overdue reporting, basic data validation). Support training documentation and administrative processes (e.g., rosters, sign-in sheets, record completion checks, internal tracking logs). Compile and summarize training data for internal reporting (e.g., completion trends, overdue training, audit requests). Perform any other tasks/duties as assigned by management.
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Job Type
Full-time
Career Level
Intern
Number of Employees
251-500 employees