Manufacturing Systems Expert

Key Responsibilities

• Define user requirement specifications by capturing and translating the voice of the customer.
• Maintain and update electronic batch records with focus on quality, cost, and timelines.
• Perform master batch record, bill of materials, and recipe updates in production systems.
• Participate in qualification and risk assessment activities for manufacturing systems.
• Validate and align technical solutions with Information Technology, Automation, and Quality teams.
• Manage manufacturing documentation updates following electronic batch record implementation.
• Ensure timely handling of deviations and change controls in compliance with regulations.
• Support shop floor operations through troubleshooting, user training, and continuous process improvement.

Essential Requirements

• Minimum five years of experience in a Good Manufacturing Practice manufacturing process support role.
• Proven experience working as a Manufacturing Execution Systems expert in a production environment.
• University degree in a scientific or technical field such as Pharmacy, Chemical Engineering, or Pharmaceutical Technology, Engineering or equivalent experience.
• Strong scientific and technical understanding with solid knowledge of automation systems.
• Good understanding of regulatory requirements across multiple health authorities and compliance standards.
• Proven ability to work collaboratively in teams, with strong adaptability and ability to perform under pressure.

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