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

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Job Description

The Pharmaceutical Sciences & Device Quality (PSDQ) function is part of Takeda’s R&D Quality organization, responsible for ensuring the highest standards of quality, compliance, and patient safety throughout the development and delivery of investigational medicines and devices. The Quality Compliance & Systems team within PSDQ provides oversight of GxP systems, inspection readiness, data integrity, and continuous improvement, ensuring adherence to global regulatory expectations and Takeda standards. 

Our division-sponsored program is designed to introduce students to a unique opportunity to work in a global pharmaceutical R&D Quality environment where compliance, systems, and innovation intersect. Students will gain hands-on experience with quality management systems, compliance processes, and digital tools that support operational excellence in pharmaceutical sciences and medical device development. The intern will be exposed to real-world challenges and collaborative projects that bridge regulatory compliance, data systems, and continuous improvement initiatives. 

How You Will Contribute: 

• 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. 

Internship Development Opportunities: 

• How global Quality Management Systems support compliance in pharmaceutical and medical device development. 

• Practical application of Good Manufacturing Practice (GMP) and other GxP regulatory requirements. 

• How to interpret and apply regulatory compliance principles to real-world quality challenges. 

• Skills in analyzing data, preparing compliance reports, and contributing to continuous improvement initiatives. 

• How to collaborate within a global, cross-functional team environment. 

Job Requirements: 

• Enrollment in a Master’s 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). 

Internship Eligibility 

• Must be authorized to work in the U.S. on a permanent basis without requiring sponsorship 

• Must be currently e