• University: NA
• College: NA
• Major: Pharmacy
• Minors: NA
• Start Date: 01 October 2019

Intern

Assisted with the review and preparation of quality control documentation to align with ICH, ISO, and MHRA regulatory standards. Supported the RA team in document tracking, version control, and compiling regulatory submissions under supervision. Developed working knowledge of global regulatory frameworks and product lifecycle management requirements. Participated in team meetings, learning the role of cross-functional collaboration in regulatory strategy and compliance. Enhanced understanding of medical device regulations within the EMEA region.

• LGBTQ: no
• Ethnicity: Asian
• Disability: no
• Veteran: no
• First-generation College Student: no
• Pell Grant Eligibility: no
• Work Authorization: no
• Visa Sponsorship: no