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Usp Data Entry Jobs in Georgia (NOW HIRING)

Usp Data Entry information

What is a USP Data Entry job?

USP Data Entry jobs involve inputting, updating, and maintaining data related to the United States Pharmacopeia (USP) standards and documentation. Professionals in this role ensure that pharmaceutical, laboratory, or related data is accurately entered into databases or software systems following USP guidelines. Their work supports compliance, quality assurance, and reporting within the pharmaceutical or healthcare industries. Attention to detail, familiarity with data management tools, and understanding of regulatory requirements are essential skills for this role.

What are some common challenges faced in a USP Data Entry role, and how can they be managed effectively?

In a USP Data Entry role, common challenges include maintaining high accuracy while handling large volumes of sensitive or technical data, meeting tight deadlines, and adapting to evolving data management systems. To manage these effectively, it's important to develop strong attention to detail, regularly double-check entries, and become proficient with the organization's specific data entry software. Collaborating closely with team members and supervisors can also help quickly resolve discrepancies and ensure data integrity.

What are the key skills and qualifications needed to thrive as a USP Data Entry professional, and why are they important?

To thrive as a USP Data Entry professional, you need strong attention to detail, fast and accurate typing skills, and a high school diploma or equivalent. Familiarity with data entry software, spreadsheets like Microsoft Excel, and sometimes specific database systems is typically required. Organizational skills, time management, and reliability help you excel in handling large volumes of information with minimal errors. These skills are crucial for maintaining data integrity, ensuring efficient workflow, and supporting accurate business operations.

What is the difference between Usp Data Entry vs Data Entry Clerk?

AspectUsp Data EntryData Entry Clerk
CredentialsBasic computer skills, data entry experienceBasic computer skills, data entry experience
Work EnvironmentOffice or remote, fast-pacedOffice or remote, administrative setting
Industry UsageCommon in healthcare, logistics, retailCommon across various industries including admin, healthcare
Job FocusEntering specific data points (e.g., USP data)General data entry tasks

Usp Data Entry and Data Entry Clerk roles share similar credentials and work environments, but Usp Data Entry often focuses on specialized data related to unique selling propositions, while Data Entry Clerks handle broader administrative data tasks across industries.

Which Usp Data Entry jobs are legit?

Usp Data Entry jobs are legitimate positions involving inputting and managing data using software tools like Excel or specialized databases. Valid jobs typically require basic computer skills, attention to detail, and sometimes a high school diploma; they are often offered by reputable companies or staffing agencies. Be cautious of scams that promise high pay for minimal work and avoid jobs that ask for upfront fees or personal financial information.

What are the most commonly searched types of Usp Data Entry jobs in Georgia?

The most popular types of Usp Data Entry jobs in Georgia are:

What cities in Georgia are hiring for Usp Data Entry jobs?

Cities in Georgia with the most Usp Data Entry job openings:

Infographic showing various Usp Data Entry job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution.

Senior Regulatory Associate -- Drugs & Biologics

The FDA Law Solution

Atlanta, GA • On-site

$100 - $130/hr

Other

Posted 4 days ago


Key responsibilities

  • Support strategy development for FDA, FTC, USDA, EPA, IND, NDA, and BLA programs.

  • Manage inspection readiness, draft responses to FDA 483s, and handle regulatory compliance documentation.

  • Coordinate with client departments and manage multiple high-priority client matters independently.


Job description

Senior Regulatory Associate — Drugs & Biologics

Location: Atlanta, GA (On‑Site) • Full‑Time • Reports to: Founder & CEO

About the Company

The FDA Law Solution, LLC. is a premier legal advisory firm specializing in navigating the complex regulatory landscape of the Food and Drug Administration. Led by industry veteran Ricky C. Benjamin, the firm provides strategic counsel to life sciences and healthcare companies to ensure product compliance and successful market entry.

Responsibilities
  • Support strategy for FDA, FTC, USDA, EPA, IND, NDA, and BLA development and commercialization programs.
  • Execute rare disease regulatory strategies including orphan drug designations.
  • Provide technical counsel on GLP‑1 compounding and USP requirements.
  • Manage inspection readiness and draft responses to FDA 483s.
  • Draft high‑level regulatory analyses and strategic client guidance memos.
  • Manage promotional and labeling review for FDA and FTC compliance.
  • Facilitate PRC and MLR meetings with minimal senior oversight.
  • Monitor post‑market compliance and adverse event reporting requirements.
  • Conduct regulatory due diligence for life science transactions and acquisitions.
  • Draft formal responses to FDA Warning Letters and enforcement actions.
  • Coordinate with client Regulatory Affairs, Quality, and Marketing departments.
  • Manage multiple high‑priority client matters independently and efficiently.
  • Participate in team meetings to align legal strategy with business goals.
  • Communicate complex regulatory concepts to non‑legal client stakeholders.
  • Maintain professional relationships with FDA project managers and officials.
Qualifications
  • Juris Doctor (JD) degree and active bar membership in good standing.
  • 5+ years of FDA regulatory law experience.
  • Proven track record in submission strategies for FDA, FTC, USDA, EPA, IND, NDA, and BLA.
  • Expert‑level legal writing, issue spotting, and regulatory analysis skills.
  • Strong scientific literacy for engagement with technical and clinical data.
  • Experience with GLP‑1 compounding (503B) and USP 797/795 standards (preferred).
  • Technical proficiency with Veeva PromoMats for promotional review (preferred).
  • Experience securing orphan drug designations for rare diseases (preferred).
  • Familiarity with REMS programs and market exclusivity strategies (preferred).
  • History of high billable efficiency with minimal time write‑offs (preferred).
Location and Working Conditions

Position is based onsite at our Atlanta, GA office. Standard business hours apply with occasional deadline‑driven intensity. Collaborative environment requiring frequent face‑to‑face engagement with the Founder. Occasional travel may be required for client site visits or inspections.

Compensation & Benefits

Competitive compensation and benefit package based on candidate's experience level.

Culture & Expectations
  • Demonstrate absolute accountability and ownership over client deliverables.
  • Maintain a solution‑oriented mindset when navigating complex regulatory barriers.
  • Exhibit professional resilience and reliability under tight agency deadlines.
  • Practice clear, respectful, and proactive communication with internal teams.
  • Align with the firm's dedication to precision and protective advocacy.
Growth & Development

This role offers a unique path to senior leadership through direct mentorship from the firm's Founder and CEO. It provides exposure to cutting‑edge specialty regulatory areas often unavailable in larger firm settings and encourages internal advancement for associates who demonstrate business savvy and commitment to expanding the firm's influence and client base.

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