Jan 09, 2023

Job Description

As an Equipment Specialist you be responsible for assigned manufacturing tasks and activities in keeping with production schedule to ensure that production is maintained to the highest standards of quality and quantity. You will also ensure that manufacturing activities are compliant with GMP, safety and environmental guidelines.

Other responsibilities:

-Suggest improvement actions (organization, process, safety, hygiene, etc.) at shop floor

Documentation Specialist GMP
-Prepare, print and consolidate the batch documents, labels... and handover to production operators within the deadlines set according to the production schedule
-Follow up on updates and versions of documents in production (procedures and logbooks)
-Manage the documents review and approval cycle
-Complete the ERP (SAP) and RFT (right first time) databases, make available and participate in the analysis of trends and performance indicators

HSE and Quality
-Promote and improve the Safety and Quality culture
-Ensure overall inspection readiness for area of responsibility
Participate in HSE risk assessments

KPI and Data Reporting for process teams
-Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt

Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Minimum Requirements

General HSE Knowledge

Knowledge of GMP

Manufacturing Process Execution


English/ German language skills
Novartis Technical Operations
Technical Operations
Full Time
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Equipment Specialist

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