Enter and Manage Deviations and CAPA as per Source Quality (Veeva System) Deviation management processes. * Assess proposed CAPA of vendors and liaise with , (Quality or business) to ensure robust CAPAs are developed and negotiate the major observations with vendors or the company business partners. * Manage, track and facilitate the project management of timely review, evidence evaluation and closure of deviations and CAPA's from deviations, audits and inspections. * Support development of Effectiveness Checks and ensure timely approval. * Preferable 5 years of experience working in the (bio)pharmaceutical industry preferred, with a minimum of 3 years in the research, clinical development or Pharmacovigilance domain. * Expertise in managing non-compliance, leading root-cause investigations, robust CAPA development and perform Effectiveness Checks in at least one of the GxPs (i.e. GcP).
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