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Zentiva

Produces branded generic pharmaceuticals in Europe

Master Data Specialist

Data EntryConfirmed live in the last 24 hours
Full-timeBucharest, RomaniaNo salary listedIn-person

About the Job

Responsibilities

  • Create material codes for all material types (FG: Fiori; SF/PM/RM/AI: SAP CEP) according to existing processes, including launches, transfers, switches, and third-party processes.
  • Maintain Master Data-specific views in SAP and ensure material workflows are closed in SAP.
  • Monitor the status of created materials, track settings, communicate with involved departments, and ensure materials are released and usable from a Master Data perspective once settings are correct and complete.
  • Generate ECRs to modify relevant GMP fields.
  • Perform a monthly cleanup of material master data settings to identify missing or incorrect settings.
  • At least twice a year, clean up master data for inactive materials with a deletion flag.
  • Extend and maintain all imported FG material codes dedicated solely to release in Bucharest.
  • Liaise directly with involved departments to resolve errors in different processes.
  • Maintain all settings required for serialization in SAP.
  • Monitor GTIN and GMID changes.
  • Monitor Master Data uploads to TraceLink.
  • Prepare the Master Data file with the local IT department and send it to the central team in Prague for upload to TraceLink for third-party customers.
  • Update the serialization file monthly according to the production plan.
  • Export Global Folders from VISTA weekly and monitor newly created VISTA folders daily, linking PM with the Global Folder.
  • Monitor FG transfers from CEP to VISTA and maintain communication with the AW and MD Central teams to resolve errors.
  • Create BOMs and BORs for FG and SF.
  • Align implementation of new BOMs created due to AW packaging changes with master planners, in accordance with the production plan and change implementation date.
  • Create BOMs and BORs according to master planners’ requirements for production work-center changes or requirements from other departments, including production and PTT where applicable.
  • Generate a monthly report on recipe-approval status covering at least two months and distribute it to internal customers.
  • Clean up recipe validity as needed in collaboration with the master planner.

About the Company

Zentiva

Produces branded generic pharmaceuticals in Europe

Zentiva makes branded generic medicines for European markets. Its products are off-patent drugs reformulated and marketed under Zentiva’s brands, delivering the same active ingredients and dosage as original medicines at lower prices. It differentiates itself through a long history as an independent platform under private equity, with a growth strategy built on acquiring brands to expand its European footprint. The goal is to become a leading European branded generics platform and improve access to affordable medicines across its markets.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Prague, Czechia
Founded
2003

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