Anunciada dia 29 novembro
Descrição
Job Description
We are seeking a skilled professional to join our R&D Quality Audit Team as a GCP Auditor. As a member of this team, you will be responsible for planning and participating in global audits of clinical trials activities, supporting regulatory inspections, and contributing to process improvement initiatives.
* Bachelor's degree in a scientific discipline or medical sciences/pharmacy qualification
* Extensive international auditing experience in GCP or as a regulatory authority inspector
* Data mining, manipulation, and data analytics skills advantageous
* Excellent written and verbal communication skills
Preferred Requirements:
* Postgraduate qualification
* Experience supporting regulatory authority inspections
* Participation in process improvement initiatives
Benefits
* Vast opportunities to learn, develop, and progress within our organization
* Diverse and inclusive community of belonging
* Generous total rewards package including healthcare, finance, wealth, and career benefits
* Flexible work arrangements
About Us
We are an equal opportunity employer and welcome applications from diverse candidates. We are committed to ensuring that individuals with disabilities have equal access to job opportunities and accommodations.
