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Description
This position supports our customer, the Food and Drug Administration (FDA) by responding to inquiries and processing electronic applications and documentation in accordance with established Standard Operating Procedures (SOPs) and business rules.
The Records Management Specialist I (Editor) primarily processes electronic documents using multiple systems. While assigned to specific core functions, individuals will be cross trained to perform additional duties based on operational needs.
Work Location: Onsite - Landover, MD
Schedule: Monday through Friday, 8:30 AM - 5:00 PM
Security Clearance: Must possess or be able to obtain a Public Trust Clearance.
Key Responsibilities
Proofreading documents for grammar, spelling, and punctuation
Editing for clarity and accuracy
Redacting confidential patient and manufacturer information in accordance
with FOIA exemptions
Injury or fatality related to medical devices
Reports submitted by healthcare providers or emergency personnel
Documentation submitted to the FDA for regulatory review
Requirements
Requirements
Two (2) years of direct document processing experience
At least one (1) year of office, records, or computer-based work experience
HeiTech Services is an Equal Opportunity Employer. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy, sexual orientation, and gender identity), national origin, age, disability, veteran status, or any other protected status under applicable law.
If you require a reasonable accommodation during the application process, please contact us at HR@HeiTechServices.com.
HeiTech Services may utilize technology-assisted tools, including artificial intelligence, to support the review of application materials. These tools are used to enhance efficiency; however, all hiring decisions are made by human reviewers in accordance with federal hiring guidelines.