Senior Manager, Regulatory Advertising & Labeling (Remote)

Nestlé S.A.; Bridgewater Township (NJ); Remote; USD 155,000 - 208,000; Full time

Benefits offered by this job

401k with company match

Healthcare coverage

Other benefits

Job summary

Nestlé Health Science is seeking a Senior Manager to own regulatory strategy for advertising, promotion, and labeling across pharmaceutical products. You will ensure communications are accurate, compliant, and aligned with current labeling while partnering with Marketing, Legal, Medical, Quality, and external agencies to enable timely launches.

This hands-on leader will drive FDA interactions, translate label changes into commercial plans, and report to the VP & Head of Global Regulatory Affairs

Qualifications

• Bachelor's degree in a scientific or regulatory field required; advanced degree preferred.
• 10+ years of regulatory affairs with hands-on advertising, labeling, or commercial regulatory work.
• Experience with Veeva PromoMats, Veeva RIM, eCTD tools and artwork workflows.
• Strong knowledge of FDA promo rules, OPDP/CBER APLB, and labeling boundaries.

Responsibilities

• Chair PRC meetings and document cross-functional decisions.
• Review and approve promotional and non-promotional materials for multiple channels.
• Ensure claims are supported by labeling and evidence.
• Provide regulatory positions with options and risk assessments.
• Lead labeling from target product profile to full company Core Data Sheet.

Skills

Regulatory affairs

FDA knowledge

Veeva PromoMats

Cross-functional leadership

Communication

Education

Bachelor's degree in science/regulatory

Tools

Veeva PromoMats

Veeva RIM

eCTD publishing

SPL/artwork workflows

Job description

Nestlé Health Science is seeking a Senior Manager to own regulatory strategy for advertising, promotion, and labeling across pharmaceutical products. You will ensure communications are accurate, compliant, and aligned with current labeling while partnering with Marketing, Legal, Medical, Quality, and external agencies to enable timely launches.

This hands-on leader will drive FDA interactions, translate label changes into commercial plans, and report to the VP & Head of Global Regulatory Affairs