Pharmaceutical Licensing Application Specialist (Puerto Rico)
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Before you apply
Salary$50k
LocationGuaynabo, PR
Work modeon-site
Typefull-time
SeniorityEntry
Experience1+ yrs
DepartmentProfessional Services
Company size8+ people
First seenOct 16, 2026 · 2w ago
Verified live21h ago
At a glanceSummarised by Seekless from the posting.
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
Experience working in a high-volume, deadline-driven environment with a strong attention to detail
Proficient in English communication, both verbal and written
Ability to interpret regulatory instructions and requirements and translate them into accurate application materials
Proficient in Microsoft Office Suite (especially Word, Excel, and Outlook)
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
Familiarity with state or federal regulatory bodies, such as Boards of Pharmacy, DEA, or FDA, is a plus
Prior experience using document management systems, customer relationship management (CRM) software, or licensing portals is preferred
Skills
Microsoft Word
Microsoft Office Suite
Microsoft Excel
Microsoft Outlook
PDF editing tools
document management systems
CRM software
licensing portals
Essential Duties and Responsibilities:
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Perform customer service and support the State Licensing department on day-to-day duties:
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Draft online and hard copy state pharmaceutical applications;
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License verification
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Review signed applications for accuracy and completion;
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Review outgoing and incoming physical mail (electronically if working remote);
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Address deficiencies highlighted by the Board on behalf of customer;
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Update internal database to reflect application progression;
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Maintain document repository of customer supporting documents, applications and deficiency correspondence;
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Administrative work (basic Microsoft Word skills required);
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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
About the role
Working Hours: Monday - Friday 8am - 4:30pm ET
About the company
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.