レベル: Associate

ジョブタイプ: Temporary

Loading ...

仕事内容

As a Master Data Quality Specialist, you are responsible for managing specifications and original documents within Quality Master Data.

Responsibilities

  • Managing and maintaining specifications in systems such as IPI and QualityDocs.
  • Drafting, modifying, approving, and archiving documents including Heist Goods Receipt Slips (HGRS) and 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).

Pay range and compensation package

  • A full-time temporary position within a professional and growing team.
  • Competitive salary with additional benefits (company car, meal & eco vouchers, hospitalization insurance, additional vacation days, etc.).
  • Opportunities for professional development and tailored training.
  • A stable working environment in the pharmaceutical sector.
Loading ...
Loading ...

締切: 24-12-2025

無料の候補者に適用するにはクリックしてください

申し込む

Loading ...

同じ仕事

Loading ...
Loading ...