Global GVP Quality Lead — Oncology R&D

BeOne Medicines; United States; Presencial; USD 143 400 - 193 400; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Comprehensive benefits package

Employee Stock Purchase Plan

Annual bonus plan

Resumo da oferta

BeOne Medicines is seeking a GVP Quality Lead responsible for overseeing Pharmacovigilance activities and ensuring compliance with regulatory requirements. The ideal candidate holds a Bachelor of Science degree and has over 8 years of experience in the field.

This role offers an exciting opportunity to shape a global GVP QA framework while working closely with senior leadership. Key tasks include conducting audits and leading inspection readiness activities.

Qualificações

• 8+ years of experience in Pharmacovigilance required.
• Expert understanding of GVPs and international regulations.
• Proven ability in driving quality process improvement initiatives.

Responsabilidades

• Support GVP Quality in compliance with regulatory requirements.
• Conduct audits and lead inspection readiness activities.
• Manage quality systems and enhance risk-based audit strategies.

Conhecimentos

Pharmacovigilance experience

Global GVP and GCP knowledge

Quality process improvement

Budgeting and finance skills

Analytical Thinking/Data Analysis

Formação académica

Bachelor of Science degree

Master’s degree

Ferramentas

Microsoft 365

Veeva

Smartsheet

Descrição da oferta de emprego

BeOne Medicines is seeking a GVP Quality Lead responsible for overseeing Pharmacovigilance activities and ensuring compliance with regulatory requirements. The ideal candidate holds a Bachelor of Science degree and has over 8 years of experience in the field.

This role offers an exciting opportunity to shape a global GVP QA framework while working closely with senior leadership. Key tasks include conducting audits and leading inspection readiness activities.