Global PV Inspection Readiness Lead

Jefferson Wells Belgium; Waals-Brabant; Hybrid; EUR 90,000 - 125,000; Full time

Job summary

Jefferson Wells Belgium is seeking an Inspection Management Lead (GVP) to join our Global Quality organization. You will lead inspection readiness and management across the global Pharmacovigilance function, ensuring compliance with GVP, GCP, and GLP while coordinating with health authorities.

Based in a collaborative, international team with Europe and the US, the role offers exposure to global regulatory inspections, cross-functional collaboration, and the opportunity to strengthen patient

Qualifications

• 5–8 years of experience in Pharmacovigilance, GVP Quality, QA or Auditing.
• Strong experience in inspection management within a regulated environment.
• Experience preparing for and supporting regulatory inspections.
• Global, cross-functional work experience.
• Solid PV and GVP expertise.
• Experience with inspections by FDA, EMA, MHRA, and other authorities.
• Background in QA and regulatory compliance.
• Audit/inspection readiness and documentation review.
• Excellent stakeholder management and collaboration skills.
• Strong written and spoken English.

Responsibilities

• Lead and coordinate inspection readiness activities across the global PV organization.
• Support and manage regulatory inspections conducted by international health authorities.
• Collaborate with PV, Regulatory Affairs, Clinical Ops and Quality teams.
• Review and assess documentation for regulatory compliance.
• Support or host inspections, including front-room and back-room activities.
• Provide quality oversight of global PV systems and processes.
• Identify compliance risks and contribute to CAPAs.
• Drive continuous improvement in inspection preparedness and quality management.

Skills

Inspection management

Pharmacovigilance

Regulatory inspections

GVP knowledge

Stakeholder management

Communication

Education

Tools

PV systems

QMS

Job description

Jefferson Wells Belgium is seeking an Inspection Management Lead (GVP) to join our Global Quality organization. You will lead inspection readiness and management across the global Pharmacovigilance function, ensuring compliance with GVP, GCP, and GLP while coordinating with health authorities.

Based in a collaborative, international team with Europe and the US, the role offers exposure to global regulatory inspections, cross-functional collaboration, and the opportunity to strengthen patient