Pharmaceutical Formulation Development Intern

Jabil•Hunt Valley, MD

6d•$16 - $32

About The Position

At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe. Summary of Program Jabil’s Summer Internship Program was recognized as one of the Top 100 Internship Programs in the country for 2025 by WayUp. This is the result of a holistic and engaging experience that summer interns at Jabil experience. As a result, interns that are a part of this program for summer 2026 will get to engage with members of Jabil’s leadership team and participate in events related to professional development, networking & socializing, and community engagement. In addition, interns will have the opportunity to work with each other in committees, be assigned a mentor, tour some of Jabil’s facilities and much more! If this sounds like a program you want to be a part of and you want to work for a company that strives to make EVERYTHING BETTER and ANYTHING POSSIBLE, then apply today. Summary of Position The Intern will provide support to the Formulation Development and Analytical R&D teams within Pii. This role is designed to assist with laboratory activities, documentation, and cross-functional projects related to formulation development, technology transfer, and analytical method development. The intern will work under the supervision of senior scientists and contribute to ongoing development programs.

Requirements

Major: Bioengineering
Class Year: Rising Junior, Rising Senior
GPA: Min 3.0
Availability: Must be available to work from May 18, 2026 - August 7, 2026
Basic understanding of pharmaceutical sciences, formulation principles, and analytical techniques.
Familiarity with laboratory safety and GMP concepts.
Effective Communication
Self-starter – Ability to drive work
Leadership Skills: Agility, Building Trusting Relationships, Decision Making Skills, & Resilience
Strong organizational skills and attention to detail.
Ability to follow written procedures and maintain accurate documentation.

Responsibilities

Assist in pre-formulation studies, excipient compatibility evaluations, and preparation of prototype formulations.
Support execution of lab-scale and pilot-scale batches, including weighing, blending, granulation, and compression activities.
Document experimental procedures and observations in compliance with internal standards
Contribute to preparation and review of technology transfer documentation (batch records, process descriptions, and reports).
Participate in data collection and organization for scale-up and manufacturing readiness.
Assist in sample preparation and execution of routine analytical tests under supervision.
Support method development and validation activities through data entry, trending, and preliminary analysis.
Maintain accurate laboratory notebooks and ensure compliance with GMP and safety requirements.