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What you'd do
- Draft clear, accurate validation protocols and summary reports in accordance with approved procedures and documentation standards.
- Support the execution of validation studies, including data collection, review, and documentation of results.
- Collaborate with cross-functional teams to support projects, investigations, and continuous improvement initiatives.
- Coordinate MSAT activities and deliverables with contractors and vendors, as needed.
- Complete required technical, safety, compliance, and role-specific training to support assigned responsibilities.
- Participate in cross-functional meetings with MSAT, Quality, Engineering, Operations, and Laboratory teams to build knowledge of biotechnology manufacturing and project execution; document action items and support timely follow-up.
- Able to work in the US and must not require sponsorship for employment visa status now or in the future (e.g., FI, H1-B status)
- A student must be currently enrolled in an accredited University or College program throughout the entire duration of the internship (Not necessarily actively taking classes)
- Available to work full-time (40 hrs./week) with reliable transportation to and from work if asked to report on-site
- Must have a minimum cumulative GPA of 2.8 or higher and be available to work the hours agreed upon with the hiring manager.
- Starts
- 2026-09-09