Manufacturing Specialist

About this role

Responsibilities

• Configure and update manufacturing execution system records to reflect site-specific master batch record design changes
• Maintain master batch record interfaces with laboratory and enterprise planning systems
• Communicate master batch record design changes with global and local cross-functional stakeholders
• Provide real-time production support to resolve master batch record issues or system workarounds
• Perform system testing with development, quality, and production teams during manufacturing execution system upgrades
• Support internal and external audits by providing system data, records, and subject matter expertise
• Ensure manufacturing execution system records align with validated equipment and cleaning requirements

Requirements

• One to three years of hands-on experience with manufacturing execution systems such as PAS-X as the primary experience if not, Emerson or Rockwell Automation
• Experience working with electronic batch record systems in regulated manufacturing environments, including pharmaceutical or comparable industries
• Practical knowledge of current Good Manufacturing Practice requirements and compliance standards
• Experience supporting or maintaining system interfaces with laboratory or enterprise planning systems
• Ability to collaborate effectively with global and local cross-functional teams
• Strong attention to detail and ability to support manufacturing activities in a production environment
• Fluency in both Spanish and English, with the ability to communicate effectively in a professional setting
• Shift work expected to cover Saturday and Sundays after initial training
• Commitment to Diversity and Inclusion
• Novartis is committed to building an outstanding, inclusive work environment and diverse team representative of the patients and communities we serve.