Development Quality Intern (Undergraduate)
About The Position
We are looking for Sophomore and Junior students majoring in Chemistry, Bioengineering, Chemical engineering, mechanical engineering, or a related field for a 12-week internship role at our Durham, NC site from May 18 2026 to August 7 2026. Position Description: Support from the Quality perspective to development Project teams and ensure delivery of quality products. Support Quality Systems transformational initiatives through Business Process Management (BPM) with a technical/digital focus. Project management and task execution for Site Improvement projects enabling the implementation digital ways of working. Site, functional and global cross collaboration and interaction (Research and Development, Global Pharmaceutical Quality Systems, IT, and others) in order to deliver digital solutions. Support in the establishment of QA requirements and monitoring Clinical Batches from the Quality Perspective. Participate in Quality audits readiness and support during quality audits, as Continuous direct compression (CDC) process for oral solid dosage products addition to inhaled products.
Requirements
- Sophomore and Junior students majoring in Chemistry, Bioengineering, Chemical engineering, mechanical engineering, or a related field
- Experience with digital tools like using electronic logbooks for training
- Enthusiasm for collaboration, cross-functional projects, public speaking, and presentation design.
- Proficiency in MS Office 365.
- Candidates must have an expected graduation date after August 2026.
- US Work Authorization is required at time of application.
- Ability to report onsite to Durham, NC 3-5 days per week.
- This role will not provide relocation assistance.
Responsibilities
- Support from the Quality perspective to development Project teams and ensure delivery of quality products.
- Support Quality Systems transformational initiatives through Business Process Management (BPM) with a technical/digital focus.
- Project management and task execution for Site Improvement projects enabling the implementation digital ways of working.
- Site, functional and global cross collaboration and interaction (Research and Development, Global Pharmaceutical Quality Systems, IT, and others) in order to deliver digital solutions.
- Support in the establishment of QA requirements and monitoring Clinical Batches from the Quality Perspective.
- Participate in Quality audits readiness and support during quality audits, as Continuous direct compression (CDC) process for oral solid dosage products addition to inhaled products.
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What This Job Offers
Career Level
Intern
Education Level
No Education Listed
Number of Employees
5,001-10,000 employees
