Senior QA Manager, eQMS

Strandassociates invites a senior QA professional to lead eQMS administration and document control within Scilife, ensuring GCP compliance across clinical trials. You will drive deviations, CAPA, and audit readiness while supporting IT validation activities in a high-growth biotech setting.

The role requires extensive GCP experience, strong English communication, and autonomous work in a fast-paced environment. Based in Belgium with options for homeworking and hybrid work arrangements.