For a pharmaceutical company in the area of Mechelen, we are looking for a Master Data Quality Specialist.
...As a Master Data Quality Specialist, you are responsible for managing specifications and original documents within Quality Master Data. Your main tasks include:
Managing and maintaining specifications in systems such as IPI and QualityDocs.
Drafting, modifying, approving, and archiving documents including:
Heist Goods Receipt Slips (HGRS)
Heist Supplier Material Specifications (HSMS)
Uploading these documents into EngageZone (or other relevant document management systems).
Ensuring compliance with pharmacopeia requirements and maintaining continuous regulatory compliance.
Initiating, reviewing, and following up on change requests.
Ensuring that Quality Master Data is accurate and up-to-date.
Evaluating and updating test methods, certificates, and related quality documentation.
Bachelor’s or Master’s degree, preferably in Life Sciences, Chemistry, Pharmacy, or a related field.
Experience in master data management within a regulated (pharmaceutical) environment.
Familiarity with document management and specification systems (such as IPI, QualityDocs, EngageZone).
Strong knowledge of pharmacopeias and change control procedures.
Highly organized with strong attention to detail.
Fluent in English (written and spoken).
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