2026 Co-Op, Deviation Investigators

Support GMP investigations for deviations, nonconformances, and atypical events by gathering data, organizing evidence, and drafting investigation content under supervision.,Assist with event triage activities (e.g., initial assessment, data requests, timeline creation, identification of impacted lots/steps/systems).,Compile and analyze information from manufacturing records, batch documentation, equipment logs, alarms, environmental monitoring trends, and QC test results.,Participate in structured root cause analysis activities (e.g., 5 Whys, fishbone, fault tree), helping document hypotheses and evidence-based conclusions.,Support development and tracking of CAPAs (corrective and preventive actions), including action definitions, owners, due dates, and effectiveness criteria.,Assist with risk assessments (as applicable) and help ensure documentation meets data integrity and quality system expectations.,Prepare clear summaries and present investigation progress or learnings in cross-functional meetings.,Identify opportunities for process/system improvements (templates, checklists, data collection methods) to increase investigation quality and efficiency.,Candidates must already hold work authorization in the US and be able to maintain that status without the need for future sponsorship.

Current student enrolled in a Bachelor's or Master's program in Engineering, Chemistry, Biochemistry, Biology, Biotechnology, Pharmaceutical Sciences, Data/Analytics, or a related field.,GPA of 3.5 on a 4 scale or equivalent (Preferred).

Bachelor's Degree, Master's Degree (current enrollment)

Must be available for the entire duration of the internship (July 13th - December 11th, 2026).,Must hold work authorization in the US without the need for future sponsorship.,This position may involve access to technology or data subject to U.S. export control laws, requiring applicants to qualify as U.S. persons (citizens, permanent residents, asylees, or refugees).