Process Documentation Specialist

Novartis · İstanbul Kurtköy, Turkey · full time · On site · July 02, 2026

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Posted July 02, 2026 · Read from Novartis
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Job Description Summary

Responsible for managing and maintaining manufacturing master data and documentation processes, including product/process routing updates, BOM creation and revision control, SAP S/4HANA key user activities, process order release and closure (TECO), and routing accuracy reporting. Oversees batch record template reviews, SOP revisions, MES batch record updates, material consumption and variance analysis, and supports technical batch release activities. Ensures documentation compliance through training delivery, readiness of shopfloor documentation systems, forms and SOPs, and manages the controlled issuance and reconciliation of forms within the CIRF system.

Skills:

  • Data Analytics
  • Digital skills
  • General HSE Knowledge
  • GMP Knowledge
  • Process excellence
  • Resilience

Skills Desired

Data Analytics

Languages:

  • English

Band

Level 3

Major accountabilities:

  • SAP S4HANA Key User
  • Product/Process Routing updates in SAP S4HANA system.
  • BOM Creation, Update/ Revision, Control & Follow-up
  • SAP order release timely, confirmation, TECO
  • RoA routing accuracy check and reporting
  • Responsible for batch record template review process; SOP reviews and revisions, batch record review
  • MES batch record revisions for basic revisions
  • Material consumptions and variance check and reporting for process orders
  • •Support process team lead for technical batch release for manufacturing; SOP periodic reviews and revisions
  • .Perform training where relevant and ensure readiness for documentation systems, forms and SOPs in shopfloor
  • Perform controlled issuance and reconciliation of forms in CIRF system

Minimum Requirements:

Work Experience:

  • Operations Management and Execution
Employer
Novartis
Location
İstanbul Kurtköy, Turkey · On site
Contract
full time