Remote Healthcare Creative QA & Compliance Lead

Power Digital Marketing; Argentina; A distancia; ARS 104.453.000 - 164.140.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Fully flex work environment: remote/in

Descripción de la vacante

Power Digital Marketing is seeking a Creative Quality & Compliance Specialist to safeguard MLR regulatory integrity of healthcare creative assets. You will gate content through pre- and post-approval QA, manage Veeva PromoMats workflows, enforce brand standards, and review copy for accuracy across digital channels.

You’ll collaborate with Creative Project Managers and client stakeholders, maintain QA documentation, and help optimize workflows using AI and the Nova ecosystem.

Formación

• 4+ years in healthcare or pharmaceutical creative production with MLR experience.
• Understanding FDA OPDP guidance and 21 CFR 202, including fair balance, ISI placement, branded vs. unbranded vs. disease‑awareness content rules, and 2253 filing requirements.
• Veeva Vault PromoMats experience (annotating, claims management, submission tracking).
• Strong eye for brand consistency, design quality, and copy accuracy across digital formats.
• Proficiency with project management tools (Asana) and collaboration across teams.

Responsabilidades

• Pre-Submission Compliance QA: Review all creative assets against MLR requirements — claims accuracy, fair balance, ISI placement, reference linking, branded vs. unbranded vs. disease-awareness rules — before they enter client Medical, Legal, and Regulatory review.
• Post-Approval QA: Final quality proof of approved assets — landing pages, ads, emails, creative — before they go live, confirming that approved content was implemented correctly and no errors were introduced in production.
• Veeva Vault PromoMats Operations: Own the hands‑on Veeva workflow — annotating assets, entering and linking claims, managing references, tracking submission status, and packaging 2253 filings.
• Brand & Design Standards Enforcement: Review creative output for visual consistency, spec adherence, and style guide compliance across all healthcare client deliverables.
• Copy Quality Review: Review all copy for grammar, tone, messaging accuracy, and alignment with approved claims and client brand voice.
• QA Process Documentation & Refinement: Build, maintain, and continuously improve the quality and compliance standards, checklists, and review processes the creative team follows.
• Creative Workflow Coordination: Support creative production operations alongside the Creative Project Manager and Account PM — maintaining Asana boards and deliverable trackers, communicating timelines and managing feedback cycles with client stakeholders, trafficking tasks between the creative team and client POCs, coordinating with cross‑channel PMs on shared deliverables, and organizing client‑provided assets within Power Digital’s file structure.
• Employ AI technologies to enhance and optimize business processes.
• Utilize and leverage Power Digital’s Nova ecosystem as it relates to your department.
• Other applicable or related duties as assigned.

Conocimientos

Quality Assurance

Veeva Vault PromoMats

Asana / PM tools

Regulatory QA

Copy Review

Herramientas

Asana

Nova ecosystem

Descripción del empleo

Power Digital Marketing is seeking a Creative Quality & Compliance Specialist to safeguard MLR regulatory integrity of healthcare creative assets. You will gate content through pre- and post-approval QA, manage Veeva PromoMats workflows, enforce brand standards, and review copy for accuracy across digital channels.

You’ll collaborate with Creative Project Managers and client stakeholders, maintain QA documentation, and help optimize workflows using AI and the Nova ecosystem.