Senior Regulatory Advertising & Labeling Lead

Nestle SA

Bridgewater (MA)

À distance

USD 155 000 - 208 000

Plein temps

14 jours+

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Résumé du poste

Nestlé Health Science is seeking a Senior Manager of Advertising, Promotion and Labeling to lead regulatory strategy and governance for promotional and labeling materials across a pharmaceutical portfolio. You will collaborate with Marketing, Medical Affairs, Legal, and Regulatory Operations to ensure compliant, commercially enabling communications.

The role requires hands-on leadership in PRC/MRL governance, FDA interactions, and lifecycle labeling from core data sheet to carton artwork, with a

Qualifications

  • Bachelor’s degree in a scientific field; regulatory or pharma focus preferred.
  • 10+ years in Regulatory Affairs with hands-on advertising/promotion experience.
  • Proficiency in Veeva PromoMats, Veeva RIM, and eCTD workflows.
  • Experience reviewing promotional materials for FDA channels.

Responsabilités

  • Lead regulatory strategy and governance for promotional, labeling, and artwork materials.
  • Review and approve materials across HCP, patient, digital, and field channels.
  • Maintain FDA submission readiness, including 2253 packages and advisory comments.
  • Manage PRC meetings, risk-based decisions, and cross-functional alignment.
  • Coordinate labeling implementation across materials and vendor content.

Connaissances

Cross-functional leadership
Regulatory strategy
Regulatory communications
Documentation & review
Attention to detail
Executive collaboration

Formation

Bachelor’s degree in science or regulatory field
Regulatory Affairs Certification (RAC) preferred

Outils

Veeva PromoMats
Veeva RIM
eCTD publishing tools
SPL/artwork workflows
Microsoft Office

Description du poste

Nestlé Health Science is seeking a Senior Manager of Advertising, Promotion and Labeling to lead regulatory strategy and governance for promotional and labeling materials across a pharmaceutical portfolio. You will collaborate with Marketing, Medical Affairs, Legal, and Regulatory Operations to ensure compliant, commercially enabling communications.

The role requires hands-on leadership in PRC/MRL governance, FDA interactions, and lifecycle labeling from core data sheet to carton artwork, with a

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