Pharmacovigilance specialist- consumer engagementNestlé
Workplace: Bulacan
Salary: Agreement
Work form: Full time
Posting Date: 28/11/2025
Deadline: 28/12/2025
Position SummaryAs 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 ManageKey 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
Regulatory & Scientific Affairs
Medical Affairs
Quality
Consumer Engagement Services
Experience and Education Requirements
Bachelor's degree in Science, Nutrition, Nursing, Pharmacy, Chemistry, or related discipline
RN, Pharmacist, Registered Dietitian, or other healthcare provider license required
3-5 years of clinical experience in a healthcare discipline
Product Safety or Pharmacovigilance experience preferred
Familiarity with Salesforce, Veeva, and SAP is a plus
Strong decision-making and prioritization skills
Preferred Skills
Working knowledge of FDA regulatory requirements
In-depth understanding of medical terminology, disease states, and treatments
Ability to interpret research literature and apply statistical concepts
Strong critical thinking, analytical, and organizational skills
Ability to work independently and meet deadlines
Excellent verbal and written communication skills
Proficiency in basic computer applications
Position SummaryAs 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 ManageKey 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
Regulatory & Scientific Affairs
Medical Affairs
Quality
Consumer Engagement Services
Experience and Education Requirements
Bachelor's degree in Science, Nutrition, Nursing, Pharmacy, Chemistry, or related discipline
RN, Pharmacist, Registered Dietitian, or other healthcare provider license required
3-5 years of clinical experience in a healthcare discipline
Product Safety or Pharmacovigilance experience preferred
Familiarity with Salesforce, Veeva, and SAP is a plus
Strong decision-making and prioritization skills
Preferred Skills
Working knowledge of FDA regulatory requirements
In-depth understanding of medical terminology, disease states, and treatments
Ability to interpret research literature and apply statistical concepts
Strong critical thinking, analytical, and organizational skills
Ability to work independently and meet deadlines
Excellent verbal and written communication skills
Proficiency in basic computer applications
Meycauayan, PH, 3020Meycauayan, PH, 3020
Nestlé
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
Regulatory & Scientific Affairs
Medical Affairs
Quality
Consumer Engagement Services
Experience and Education Requirements
Bachelor's degree in Science, Nutrition, Nursing, Pharmacy, Chemistry, or related discipline
RN, Pharmacist, Registered Dietitian, or other healthcare provider license required
3-5 years of clinical experience in a healthcare discipline
Product Safety or Pharmacovigilance experience preferred
Familiarity with Salesforce, Veeva, and SAP is a plus
Strong decision-making and prioritization skills
Preferred Skills
Working knowledge of FDA regulatory requirements
In-depth understanding of medical terminology, disease states, and treatments
Ability to interpret research literature and apply statistical concepts
Strong critical thinking, analytical, and organizational skills
Ability to work independently and meet deadlines
Excellent verbal and written communication skills
Proficiency in basic computer applications
Position SummaryAs 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 ManageKey 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
Regulatory & Scientific Affairs
Medical Affairs
Quality
Consumer Engagement Services
Experience and Education Requirements
Bachelor's degree in Science, Nutrition, Nursing, Pharmacy, Chemistry, or related discipline
RN, Pharmacist, Registered Dietitian, or other healthcare provider license required
3-5 years of clinical experience in a healthcare discipline
Product Safety or Pharmacovigilance experience preferred
Familiarity with Salesforce, Veeva, and SAP is a plus
Strong decision-making and prioritization skills
Preferred Skills
Working knowledge of FDA regulatory requirements
In-depth understanding of medical terminology, disease states, and treatments
Ability to interpret research literature and apply statistical concepts
Strong critical thinking, analytical, and organizational skills
Ability to work independently and meet deadlines
Excellent verbal and written communication skills
Proficiency in basic computer applications
Meycauayan, PH, 3020Meycauayan, PH, 3020
Nestlé
Other Info
Meycauayan City, Bulacan
Permanent
Full-time
Permanent
Full-time
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