Pharmacovigilance QA Auditor - Global Compliance & PV Expert

Johnson & Johnson Co.; Singapore; On-site; SGD 60,000 - 100,000; Full time

Job summary

Johnson & Johnson is seeking a Pharmacovigilance Auditor focused on QA audits and regulatory readiness across global locations. You will support inspections, trainings, and cross‑functional projects to ensure PV compliance and risk management.

The role requires PV experience, QA auditing expertise, and strong analytical and communication skills to collaborate with partners worldwide. A Bachelors in life sciences is preferred, with regional regulatory knowledge a plus.

Qualifications

• Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related discipline.
• Minimum 2 years of experience in Pharmacovigilance (PV) within the pharmaceutical or biotech industry.
• 2+ years of QA auditing experience, specifically in Pharmacovigilance / GVP audits (preferred).
• Knowledge of PV regulations and guidelines including EU GVP and Health Authority requirements in Asian countries.

Responsibilities

• Leads the planning, conduct and reporting of PV QA audits in line with GxP/regulatory requirements.
• Supports regulatory inspections in various roles.
• Completes assigned PV training requirements to ensure inspection readiness.
• Participates in projects or teams, ensuring milestones and timelines are met.
• Provides consultation to business partners on routine tasks and helps resolve non-routine issues.

Skills

Analytical thinking

Attention to detail

Regulatory liaison

Cross-functional collaboration

Communication skills

Stakeholder influence

Global work experience

Education

Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related discipline

Job description

Johnson & Johnson is seeking a Pharmacovigilance Auditor focused on QA audits and regulatory readiness across global locations. You will support inspections, trainings, and cross‑functional projects to ensure PV compliance and risk management.

The role requires PV experience, QA auditing expertise, and strong analytical and communication skills to collaborate with partners worldwide. A Bachelors in life sciences is preferred, with regional regulatory knowledge a plus.