2026 U.S. Summer Internship Program: Pharmaceutical Sciences & Device Quality (PSDQ) Quality Compliance & Systems Intern (R&D Quality)

Role Summary

2026 U.S. Summer Internship Program: Pharmaceutical Sciences & Device Quality (PSDQ) Quality Compliance & Systems Intern (R&D Quality)

Responsibilities

• Support quality compliance activities, including tracking of Quality Events, CAPAs, and inspection readiness tasks.
• Assist with analysis, monitoring, and improvement of global Quality Systems (e.g., Veeva QMS, metrics dashboards).
• Contribute to regulatory intelligence and policy/SOP review activities.
• Participate in preparation of materials for internal audits, management reviews, and governance forums.
• Collaborate with PSDQ stakeholders on digital and data-driven initiatives to increase efficiency and transparency.

Qualifications

• Enrollment in a Master‚Äôs program in Pharmacy, Pharmaceutical Sciences, Quality Management, Regulatory Affairs, Biomedical Sciences, or related discipline.
• Foundational understanding of GxP regulations and quality principles preferred.
• Demonstrated ability to work effectively as a collaborative team member.
• Strong analytical, organizational, and communication skills.
• Proficiency in Microsoft Office; exposure to data visualization tools (e.g., Power BI) is a plus.
• This internship requires full-time commitment during the summer program (on-site/hybrid as applicable).

Education

• Master‚Äôs program or equivalent in related field as specified above.

Additional Requirements

• Must be authorized to work in the U.S. on a permanent basis without requiring sponsorship.
• Must be currently enrolled in a degree program graduating December 2026 or later.
• The internship program is 10-12 weeks depending on the two start dates (May 26th-August 14th or June 15th- August 21st).
• The intern must be able to commit to one of these time frames.
• Able to work full time 40 hours a week during internship dates.