2027 Future Talent Program - Global Regulatory Affairs & Compliance US Subsidiary - Intern
Merck · Rahway, NJ
RegulatoryFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
This 12-week summer internship with Merck's Global Regulatory Affairs and Clinical Safety team focuses on drug shortages and regulatory support. The intern will support FDA interactions, regulatory intelligence, and supply resiliency initiatives while gaining hands-on experience in pharmaceutical regulatory affairs.
What they're looking for
- Currently pursuing Bachelor of Science or Doctor of Pharmacy degree
- Enrolled in accredited college or university, returning after internship
- Demonstrated interest in pharmaceutical industry, healthcare, regulatory affairs, or life sciences
- Strong analytical, problem-solving, and critical-thinking abilities
- Excellent written and verbal communication skills
- Proficiency in Microsoft Office applications including Excel and PowerPoint
- Ability to work independently and collaboratively in team settings
What you'll be doing
- Monitor and analyze U.S. drug shortage regulations, FDA communications, and emerging regulatory trends
- Assist with maintaining internal resources, playbooks, procedures, and training materials
- Conduct research and regulatory intelligence assessments on drug shortages and supply continuity
- Support departmental digital innovation and automation projects for business process improvements
- Develop presentations, reports, and communication materials for internal stakeholders
Compensation$39,108–$111,111
Privacy & handoff
This role links to Merck's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.