Lead and manage comprehensive quality audits across Good Clinical Practice (GCP), Pharmacovigilance (GVP), and other GxP environments, both internally and at external partner sites worldwide. This role takes full ownership of the audit lifecycle—from planning and execution to reporting and follow-up on corrective actions—ensuring alignment with global regulatory standards.
Key Responsibilities
- Conduct risk-based audits across GMP, GDP, GCP, GVP, and GCLp settings, adapting approach to evolving project and regulatory needs
- Serve as a recognized expert in quality assurance, providing guidance during regulatory inspections and internal reviews
- Develop and refine audit practices by mentoring junior auditors and reviewing peer performance
- Collaborate with the Global Quality Audit team to strengthen audit frameworks and enhance compliance strategies
- Travel frequently across regions to support on-site assessments and build strong cross-functional relationships
What You Bring
- Proven background in auditing one or more GxP disciplines, with formal Lead Auditor certification
- Degree or equivalent experience in a scientific or healthcare-related field
- Strong ability to operate independently within complex, global organizations
- Fluency in English; French language proficiency is an asset
- Willingness to travel internationally on a regular basis
Our Commitment to You
We foster a culture built on collaboration, precision, and human-centered leadership. Here, your perspective matters. We value diversity of thought and experience, support inclusion at every level, and empower individuals to grow authentically. Your work will directly contribute to advancing patient-centered initiatives and improving outcomes through high-quality standards.
This is a remote position offering flexibility and global engagement, with expectations for significant travel to support on-site audit activities. We provide accommodations throughout the hiring process and are dedicated to ensuring all team members feel supported and heard.
