Master data quality specialist

• key responsibilities

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.
• qualifications
• 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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