Skip to the page

Pharmaceutical Licensing Application Specialist (Puerto Rico)

LighthouseAIRipplingGuaynabo, Puerto Rico, United States
Posted 17 SepFound 20 OctSeen 4 hours ago

Fit

The keywords the posting names, against what your resume says.

Add your resume to see which of its keywords you already have, and get a resume tailored to this posting. 10 a month, free.

The Posting

About LighthouseAI
LighthouseAI, a Pharma Solutions company, provides state licensing software and professional services to pharmaceutical and medical device manufacturers, wholesale distributors, third-party logistics providers (3PLs), and pharmacies. Our software identifies the licensing requirements that apply to each facility, monitors regulatory change, and tracks every license and renewal across 56 US jurisdictions. Our 35+ veteran licensing professionals handle filings, renewals, and agency communication. Since 2015, we have served 700+ clients and today manage 13,000+ licenses for 250+ active clients.

Essential Duties and Responsibilities:

  • Perform customer service and support the State Licensing department on day-to-day duties:
  • Draft online and hard copy state pharmaceutical applications;
  • License verification
  • Review signed applications for accuracy and completion;
  • Review outgoing and incoming physical mail (electronically if working remote);
  • Address deficiencies highlighted by the Board on behalf of customer;
  • Update internal database to reflect application progression;
  • Maintain document repository of customer supporting documents, applications and deficiency correspondence;
  • Administrative work (basic Microsoft Word skills required);
  • Responsibilities and tasks outlined in this document are not exhaustive and may change as determined by the needs of the company and/or its customers.

Work Experience Qualification:

  • Minimum of one (1) year of experience in regulatory affairs, licensing, or a related administrative field, preferably in the pharmaceutical, healthcare, or life sciences industries.
  • Demonstrated experience with regulatory data entry, application processing, or compliance documentation.
  • Familiarity with state or federal regulatory bodies, such as Boards of Pharmacy, DEA, or FDA, is a plus.
  • Experience working in a high-volume, deadline-driven environment with a strong attention to detail.
  • Prior experience using document management systems, customer relationship management (CRM) software, or licensing portals is preferred.

Other Qualifications:

  • Proficient in English communication, both verbal and written, with the ability to craft professional emails and produce clear, well-structured documentation.
  • Ability to interpret regulatory instructions and requirements and translate them into accurate application materials.
  • Proficient in Microsoft Office Suite (especially Word, Excel, and Outlook); experience with PDF editing tools is a plus.
  • Capable of handling sensitive or confidential information with discretion.
  • Highly organized with the ability to prioritize and manage multiple tasks simultaneously.
  • Self-motivated, adaptable, and comfortable working independently or collaboratively in a remote or hybrid environment.
  • Demonstrated problem-solving ability and a proactive approach to addressing application deficiencies or process delays.

Compensation: $50,000 annual salary

Location: This position is on-site in Guaynabo, Puerto Rico

Working Hours: Monday - Friday 8am - 4:30pm ET

Facts

Source
Rippling
External id
27176114-1a6d-4069-a859-6912b5f92549
Location
Guaynabo, United States
Remote
On-site, from the posting
Employment
Full time
Posted
17 Sep 2026, 17:15
First seen
20 Oct 2026, 10:18
Last seen
1 Nov 2026, 02:00
Status
Not yet added
Posting id
7467d945-e43f-5c76-acac-76900dc8b7d7