Veeva Systems, Inc. is seeking a Clinical Compliance Operations Specialist to drive GCP project audits and uphold quality processes across multi-line products and regulated domains.
The role collaborates with global teams to promote GCP compliance, author GxP documents, and manage incident remediation. The ideal candidate has 3+ years in Clinical QA within Life Sciences, strong technical writing, and a proven ability to navigate ISO 9001/QSRs, GCP guidelines, and CAPA programs in a fast-paced
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GCP Compliance & Quality Operations Specialist in London employer: Veeva Systems, Inc.
Veeva Systems is an exceptional employer, offering a dynamic work culture that prioritises employee success and flexibility, allowing you to thrive in your preferred environment, whether at home or in the office. With a commitment to diversity and inclusion, Veeva fosters a supportive atmosphere where employees can grow through meaningful work in the life sciences sector, backed by comprehensive benefits such as private health insurance and flexible paid time off. Join us in making a positive impact on the industry while enjoying the unique advantages of being part of a pioneering public benefit corporation.
