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

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 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  

Program Highlights:

• Hands-on experience with real projects and responsibilities 

• Dedicated mentorship program pairing interns with experienced professionals 

• Networking opportunities with industry professionals and fellow interns 

• Internship events focused on professional and skills development  

• Exposure to multiple business areas or departments within a Pharmaceutical Organization 

Applications will be accepted between October 31st- November 16th