Global PV Quality Lead – Associate Director

BeiGene; United States; Remote; USD 143,000 - 193,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401(k)

Paid Time Off

Wellness program

Employee stock purchase plan

Equity awards

Job summary

BeOne Medicines Ltd. is seeking a General Description Good Pharmacovigilance Practice (GVP) Quality Lead to support the Director, GVP Quality, in building a proactive, global GVP QA program.

You will help ensure PV activities comply with regulations, governing bodies and internal standards to improve inspection readiness and regulatory success. The role emphasizes audit leadership, risk management, vendor oversight, KPI development, and cross-functional leadership across a growing oncology

Qualifications

• Bachelor of Science degree required.
• Master’s degree preferred.
• Expert global knowledge of GVPs and GCP requirements.
• Understanding of international regulations for clinical trials and pharmacovigilance.

Responsibilities

• Audit & Inspection Leadership responsibilities for PV activities.
• Quality Systems & Risk Management oversight.
• Manage routine/audit activities for vendors and partners.

Skills

GVP knowledge

GCP knowledge

Problem solving

Leadership

Regulatory compliance

Education

Bachelor of Science degree

Master’s degree

Tools

Microsoft 365

Veeva

SumTotal

ACE Audit utopia

Smartsheet

Job description

BeOne Medicines Ltd. is seeking a General Description Good Pharmacovigilance Practice (GVP) Quality Lead to support the Director, GVP Quality, in building a proactive, global GVP QA program.

You will help ensure PV activities comply with regulations, governing bodies and internal standards to improve inspection readiness and regulatory success. The role emphasizes audit leadership, risk management, vendor oversight, KPI development, and cross-functional leadership across a growing oncology