Specialist, Regulatory Affairs
Merck · De Millsboro, DE
RegulatoryFull-time$87k–$137kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Merck seeks a Regulatory Affairs Specialist to support animal health product filings and compliance with USDA regulations. Based in Delaware with collaboration across global teams, the role manages project coordination, documentation, and regulatory submissions for both new and marketed products.
What they're looking for
- Bachelor's degree with minimum 3 years regulatory experience
- Experience in regulated industries: pharmaceutical, animal health, biotech, medical device, or food
- Familiarity with regulatory agencies and compliance processes
- Proficiency in Microsoft Office, Excel, Teams, and SharePoint
- Experience with project management software and reporting tools
- Strong organizational and time management skills for multiple priorities
- Excellent communication and cross-functional collaboration abilities
What you'll be doing
- Maintain spreadsheet-based trackers for project timelines, submissions, and regulatory milestones
- Track concurrent projects and deadlines while communicating schedule updates to stakeholders
- Coordinate with internal teams and external agencies to support submission activities and information requests
- Organize project documentation and facilitate communication using Microsoft Teams and SharePoint
- Support document control, records management, and regulatory compliance activities
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.