Regulatory Submissions Editor & Strategy Lead

Altria; Richmond (VA); Hybride; USD 133 000 - 202 000; Plein temps

Avantages offerts par ce poste

Hybrid work schedule

Paid time off

Holidays

401(k) plan with company match

Professional development stipends

Résumé du poste

Altria in Richmond, VA is seeking a Senior Manager and Editor, Regulatory Submissions Strategy to join its Regulatory Affairs Organization. The role develops, writes, edits, and proofs complex regulatory content, including FDA submissions, translating scientific detail into clear, compliant materials for senior leadership and project teams.

You will drive submission strategy for large-scale documents, manage stakeholders, supervise contract editors, and ensure timely delivery with strict

Qualifications

• Bachelor's degree in a regulatory, scientific, legal, or related field required; advanced degree preferred.
• 8+ years of relevant experience writing or editing business, public affairs, regulatory, scientific, or legal documents.
• Working knowledge of FDA processes and requirements; direct experience developing FDA submissions strongly preferred.
• Advanced written and editorial skills, with exceptional attention to detail and a strong command of grammar, style, and usage.
• Demonstrated ability to synthesize complex scientific and technical information using excellent critical-thinking skills.
• Proven ability to influence without authority and to collaborate effectively across broad and diverse stakeholder groups.
• Strong project management and organizational skills, with a proven ability to manage competing priorities and consistently meet timelines.
• Proficiency with Microsoft Word, PowerPoint, and Sharepoint; familiarity with electronic document management and regulatory publishing systems (e.g., eTTD) preferred.
• Demonstrated ability to use Cowork and other AI tools to increase efficiency.
• RIM tool experience preferred.

Responsabilités

• Participate in development of strategy for large-scale FDA submission documents.
• Write and edit submission documents, effectively integrating science and advocacy into clear, accurate, and compliant communications.
• Edit and proofread a range of content - including printed materials and slide presentations - to ensure clarity, accuracy, consistency, and application of required editorial style.
• Ensure timely delivery of consistent, high-quality, accurate, and complete written materials, maintaining quality and version control across large-scale documents.
• Manage internal stakeholder relationships with scientists, senior management, project managers, and science authors to deliver the best written product.
• Supervise and coordinate contract editorial resources as needed to meet submission timelines and quality standards.

Connaissances

Regulatory writing

Editorial skills

Project management

Stakeholder management

Attention to detail

Cross-functional collaboration

Formation

Bachelor's degree in regulatory/scientific/legal or related field

Outils

Microsoft Word

PowerPoint

SharePoint

eTTD regulatory publishing

Cowork AI tools

RIM tools

Description du poste

Altria in Richmond, VA is seeking a Senior Manager and Editor, Regulatory Submissions Strategy to join its Regulatory Affairs Organization. The role develops, writes, edits, and proofs complex regulatory content, including FDA submissions, translating scientific detail into clear, compliant materials for senior leadership and project teams.

You will drive submission strategy for large-scale documents, manage stakeholders, supervise contract editors, and ensure timely delivery with strict