The Regulatory Operations Specialist’s main responsibility is to manage regulatory submissions and associated tasks for 1-3 client brands while following industry standards, as well as agency-and client-established processes. The Specialist will partner with agency brand teams to help prepare and upload submission materials into client submission portals. This role requires excellent planning, problem-solving, organizational, written, and verbal communication skills to ensure accuracy and efficiency of submissions, as well as the ability to work in a fast-paced, deadline-driven environment.

The Specialist must be a critical thinker and be able to learn new systems and processes for the agency and their assigned client brands. Proficiency in Excel, Word, PowerPoint, Outlook, and Teams required.

Responsibilities:

- Successfully manages day-to-day workload for 1-3 client brands.
- Stays up-to-date on the latest standard operating procedures for each assigned client brand.
- Prioritizes workload to successfully meet each client's deadline.
- Communicates clearly and effectively with appropriate agency team members about status, requirements, and challenges when working on submissions.
- Maintains updated trackers and assist on updating client brand process decks.
- Communicates changes in processes to the extended internal teams.
- Attends agency team meetings for assigned client brands.
- Complies with agency administrative processes and ways of working.
- Uploads clean,



properly named documents, and annotated pieces with appropriate references.
- Opens placeholders for submissions as required by client process. Flag missing information (metadata) to the account team where applicable.
- Responsible for resubmissions, final submissions, validation, and functional annotations, as specified by assigned client brands’ regulatory process needs.
- Uploads relevant supporting documents to accompany submissions.
- Links tactics to relevant component assets as per assigned client brands’ regulatory process.
- Tracks status of submitted tactics in the MLR portal.
- Downloads MLR comments from submission portal and share with account, project management, and copy.
- Uploads references and assets to the submission portal for approval.

Requeriments

- 1+ year of experience in the Pharma or Legal industry.
- Strong attention to detail.
- Advanced English proficiency (B2+ or C1).
- Proficiency in Microsoft Office and Google Workspace.

Benefits

- Contribute to a culture of operational excellence
- Work on high-impact projects
- Dynamic and collaborative environment with professional growth opportunities
- Adaptable work environment with a strong work–life balance
- Stability and wellness programs, including:
- Private health insurance support
- Employee fund
- Additional paid time off, including half a day off on your birthday ?
- Hybrid work model

📌 Regulatory Ops Specialist (Bogotá)
🏢 Omnicom Global Solutions Colombia
📍 Bogotá