Oxford Global Resources is looking for a Compliance Engineer profile for a pharmaceutical client in Geel, Belgium. It is a temporary project of 6 months.
Responsibilities:
* QMS action management: Create and follow up actions in the QMS system (VeeVa) within the Engineering & Maintenance department.
* Technical root cause analysis: Serve as the central contact for performing technical root cause analyses of deviations across diverse systems (process systems, HVAC, clean utilities such as WFI, ROW, process gases, etc.).
* CAPA development: Support the drafting and follow‑up of CAPAs.
* Cross‑functional coordination: Collaborate closely with stakeholders such as Production, QA, and system owners.
* Quality capability building: Contribute to quality upskilling within the E&M department and help monitor quality‑related KPIs.
Requirements:
* QMS experience, ideally, experience working with Quality Management Systems in a compliance‑oriented role.
* Technical problem‑solving, ability to analyse technical deviations across multiple system types.
* Stakeholder collaboration, comfortable working with cross‑functional teams such as QA, Production, and system owners.
If you are interested in this opportunity and believe your experience aligns with the role, please feel free to share your CV or reach out for more information. We look forward to hearing from you and discussing the next steps.