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Creative Quality & Compliance Specialist (Healthcare)

Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Creative Quality & Compliance Specialist (Healthcare): Reviewing and preparing healthcare creative assets for MLR compliance, brand consistency, copy accuracy, and launch readiness with an accent on Veeva Vault PromoMats, FDA requirements, and 2253 submission packaging. Focus on establishing repeatable QA checkpoints, managing claims and references, refining compliance standards, and coordinating creative workflows without introducing regulatory or production errors.

Location: Remote - United States; candidates must be legally eligible to work in the U.S.

Company

hirify.global is an AI-native growth firm combining strategic, creative, analytical, and technology expertise to help brands improve measurable business outcomes.

What you will do

  • Review healthcare creative assets, including ads, landing pages, emails, social content, and video, for MLR compliance before submission and launch.
  • Verify claims accuracy, fair balance, ISI placement, reference linking, content classification, brand standards, design quality, and copy accuracy.
  • Operate Veeva Vault PromoMats by annotating assets, managing claims and references, tracking submissions, and packaging 2253 filings.
  • Perform final post-approval QA to confirm approved content was implemented correctly before publication.
  • Build and maintain QA checklists, compliance reference guides, brand review criteria, and repeatable review processes.
  • Coordinate deliverable tracking, feedback cycles, task trafficking, client-provided assets, and shared deliverables with project managers and client stakeholders.

Requirements

  • 4+ years of healthcare or pharmaceutical creative production experience in an agency or in-house environment.
  • Direct experience with MLR review workflows and understanding of FDA OPDP guidance and 21 CFR 202, including fair balance, ISI placement, branded and unbranded content rules, disease-awareness content, and 2253 filings.
  • Strong attention to brand consistency, design quality, copy accuracy, and digital creative specifications.
  • Ability to document, maintain, and independently improve QA standards and review processes.
  • Ability to provide clear, actionable feedback to designers, copywriters, freelancers, and project teams.
  • Proficiency with Asana or comparable project management platforms and experience in a fast-paced agency environment.

Nice to have

  • Veeva Vault PromoMats experience or certification.
  • Experience with modular content strategies.
  • Experience supporting both pharma-regulated and non-regulated healthcare clients.

Culture & Benefits

  • Fully flexible work environment supporting remote, in-office, and hybrid work for employees legally eligible to work in the U.S.
  • Base salary with commission opportunities.
  • Medical, dental, and vision insurance with up to 100% employer contribution toward the employee monthly premium.
  • 401(k) plan with a 4% employer contribution match and unlimited time off from day one.
  • Paid volunteer time, employee assistance, U.S. national holidays, mental health recharge days, and professional development programs.
  • AI technologies and the Nova ecosystem are used to improve business processes.

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