Europe Deputy QPPV & Pharmacovigilance Lead

Revolution Medicines

Amsterdam

On-site

EUR 120,000 - 155,000

Full time

14 days+
Application generator

An application made for this job — a tailored resume and cover letter that speak straight to the posting.

Get past ATS filters

Job summary

Revolution Medicines is seeking an experienced EU Deputy QPPV to join our dynamic team and report to the QPPV. You will support the oversight, maintenance, and continuous improvement of our European pharmacovigilance system, ensuring compliance with EU pharmacovigilance legislation and GVP.

As Deputy EU QPPV, you will stand in for the EU QPPV, maintain awareness of safety issues and regulatory inspections, and collaborate with EMA and national authorities to ensure 24/7 availability of the QPPV

Qualifications

  • Advanced degree in life sciences with relevant field.
  • 7–9+ years in international pharmacovigilance; PV quality focus.
  • Experience managing global PV systems and health authority interactions.
  • Fluent in English; second European language is a plus.

Responsibilities

  • Support EU QPPV in maintaining PV system and PSMF.
  • Act as deputy EU QPPV during QPPV absence.
  • Coordinate safety governance, signal management and risk assessments.
  • Assist with regulatory interactions (EMA, NCAs).
  • Support inspections readiness and CAPA tracking.
  • Ensure 24/7 availability arrangements for EU QPPV.

Skills

EU pharmacovigilance
PV quality & compliance
PV systems
Communication skills
Leadership
Problem solving
Biotech environment

Education

Advanced degree in life sciences

Tools

PV databases
PSMF management

Job description

Revolution Medicines is seeking an experienced EU Deputy QPPV to join our dynamic team and report to the QPPV. You will support the oversight, maintenance, and continuous improvement of our European pharmacovigilance system, ensuring compliance with EU pharmacovigilance legislation and GVP.

As Deputy EU QPPV, you will stand in for the EU QPPV, maintain awareness of safety issues and regulatory inspections, and collaborate with EMA and national authorities to ensure 24/7 availability of the QPPV

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Senior Pharmacovigilance Alliance Lead (Hybrid)
Senior Pharmacovigilance Alliance Lead (Hybrid)

ProPharma Group • Leiden

Hybrid
EUR 90,000 - 120,000
Senior Pharmacovigilance Consultant, Alliance Management
Senior Pharmacovigilance Consultant, Alliance Management

ProPharma Group • Leiden

Hybrid
EUR 90,000 - 120,000
Senior Pharmacovigilance Consultant, Alliance Management
Senior Pharmacovigilance Consultant, Alliance Management

ProPharma • Leiden

Hybrid
EUR 70,000 - 90,000
Senior PV Alliance Manager (Hybrid)
Senior PV Alliance Manager (Hybrid)

ProPharma • Leiden

Hybrid
EUR 70,000 - 90,000
Senior Director, Pharmacovigilance & Safety Operations
Senior Director, Pharmacovigilance & Safety Operations

uniQure • Amsterdam

On-site
EUR 150,000 - 190,000
Senior Director, Safety Operations
Senior Director, Safety Operations

uniQure • Amsterdam

On-site
EUR 150,000 - 190,000
Pharmacovigilance & Regulatory Affairs Officer
Pharmacovigilance & Regulatory Affairs Officer

ALK • Almere

Hybrid
EUR 55,000 - 75,000
Hybrid work model
Exposure to PV/RA across Benelux/UK
Director of Regulatory Affairs
Director of Regulatory Affairs

QTC Recruitment • Netherlands

On-site
EUR 90,000 - 120,000
Competitive compensation package
Long-term development potential
Dynamic working environment
VP Quality 17-11-2025 25-11-2025
VP Quality 17-11-2025 25-11-2025

Prothya Biosolutions Netherlands B.V • Amsterdam

Hybrid
EUR 180,000 - 260,000
Senior QA & QP Leader - EU GMP & Clinical Supply
Senior QA & QP Leader - EU GMP & Clinical Supply

Rhythm Pharmaceuticals Inc. • Amsterdam

Hybrid
EUR 120,000 - 160,000
Hybrid work model