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Pharmaceutical Manufacturing

Pharmaceutical Licensing Application Specialist (Puerto Rico)

Guaynabo, PROnsiteFull TimeEntry-level (exp-based)$50,000–$50,000 /yrPosted 1 month ago

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Required skills

  • pharmaceutical applications
  • license verification
  • application processing
  • regulatory data entry
  • compliance documentation
  • Microsoft Office Suite
  • Word
  • Excel
  • Outlook
  • English communication

Nice to have

  • document management systems
  • CRM software
  • licensing portals
  • PDF editing tools
  • Boards of Pharmacy
  • DEA

Role summary

The Pharmaceutical Licensing Application Specialist will support the State Licensing department by drafting and processing pharmaceutical applications, verifying licenses, and ensuring accuracy and completion. This role involves updating internal databases, maintaining document repositories, and addressing deficiencies highlighted by regulatory boards. The specialist will also perform administrative tasks, requiring proficiency in Microsoft Office Suite, particularly Word, Excel, and Outlook. The position emphasizes strong attention to detail, organizational skills, and the ability to work in a high-volume, deadline-driven environment. Familiarity with regulatory bodies and document management systems is preferred. This is an on-site role in Guaynabo, Puerto Rico.

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

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