Pharmacovigilance Specialist- Consumer Engagement

Benefits

Parental leave

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Non-birth-parent leave

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Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

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Relocation assistance

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Childcare support

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Learning budget

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Verification

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Salary

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Market context

U.S. role benchmark (BLS OEWS)

$81,444 U.S. median for this role

Projected growth (BLS Employment Projections)

+6.9% - Faster than average

Matched to SOC 29-1141 - Healthcare aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function

Healthcare From the posting source checked Jun 20, 2026

Seniority

Mid From the posting source checked Jun 20, 2026

Schedule

Shift type

Not verified

Weekend work

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Company

Company stage

Public-company From the posting source checked Jun 20, 2026

Application

Cover letter

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Assessment

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Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Pharmacovigilance Specialist- Consumer Engagement Country Philippines Position Summary As a Specialist, Pharmacovigilance , you will play a critical role in ensuring the safety and compliance of Nestle's VMS, Cosmetic, and OTC products You will manage adverse event case reviews, documentation, assessments, and MedWatch submissions in line with FDA regulatory guidelines. This position also supports Medical Nutrition products, collaborates with Medical Affairs, and contributes to product lifecycle improvements through scientific analysis and hypothesis generation. You will work closely with cross-functional teams including Regulatory & Scientific Affairs, Medical Affairs, Quality, and Consumer Engagement Services, reporting directly to the Pharmacovigilance Manage Key Responsibilities Review and assess adverse events daily for NHSc VMS brands in compliance with DSCPA. Conduct follow-up intakes with consumers and healthcare entities via phone, mail, or electronic channels, ensuring accurate documentation. Complete serious adverse event narratives using MedWatch Form 3500A and report to FDA within 15 days. Code adverse events by System Organ Classification in Salesforce for trend analysis. Initiate product reviews or investigations based on hypotheses or events of concern. Maintain up-to-date knowledge of FDA guidelines, regulatory requirements, and internal procedures. Stay informed on nutrients, ingredients, and structure-function claims. Perform other duties as assigned. Key Relationships NHSc US Regulatory Operations & Compliance team Regulator

Read the full description at jobdetails.nestle.com. FewerJobs shows a preview and links to the original posting.