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As our new quality assurance specialist, you play an essential role in optimizing our document and training workflows. You get to champion cGMP compliance while working alongside an empowering team that values your professional development. In this dynamic quality assurance specialist position, you will see your direct impact on patient safety and product quality every single day.
Job Responsibility
Manage the DPDS Beerse controlled document lifecycle as an expert business administrator in Truvault
Deliver engaging Truvault and Summit system training sessions to empower new users and contractors
Maintain the Learning Management System to track training files, ensure compliance, and support operational departments
Author and review critical GMP procedures to align with corporate standards and regulatory requirements
Assist with proactive preparations for internal audits and global regulatory inspections
Requirements
Bachelor degree in life sciences or equivalent transferable experience
one to three years of successful experience in a regulated pharmaceutical environment
strong organizational capabilities paired with high precision and accuracy
fluent in English
familiarity with GMP regulations and eagerness to learn new quality systems