Merck Seeks Interns for Regulatory Planning and Publishing Role
Merck has opened applications for its Regulatory Planning and Publishing Intern position, specifically targeting undergraduates who receive Pell grants and can commute to Rahway, New Jersey. This opportunity is part of Project Onramp and is set to begin in the summer of 2027. The internship focuses on the critical process of preparing drug applications for global health authorities such as the FDA and EMA. Interns will work with cross-functional teams to build project timelines, track data submissions, and format technical documents into the industry-standard electronic Common Technical Document (eCTD) format.
The role offers hands-on experience in understanding how life-saving medicines navigate regulatory pathways from clinical trials to market. Merck is seeking candidates who are quick learners, can multitask effectively, and adapt to a fast-paced environment with shifting priorities. Ideal candidates should also demonstrate self-advocacy and resourceful problem-solving skills.
Proficiency in advanced features of Microsoft Office 365 programs, including SharePoint, Teams, Outlook, Word, PowerPoint, and Excel, is required. Additionally, candidates should have experience with automation, artificial intelligence (AI), data analysis, and digital technologies to improve business processes and operational efficiency. A GPA of 3.0 or higher is also necessary for consideration.
The application period for this internship began on October 6, 2026, and will close on October 23, 2026. This program represents a unique opportunity for students to bridge the gap between pharmaceutical science and government compliance while gaining valuable experience in the regulatory planning and publishing field.