Manufacturing Systems Lead for MES & Digital Transformation

Novartis

Fatih

On-site

TRY 180,000 - 240,000

Full time

14 days+
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Job summary

Novartis is seeking a Manufacturing Systems Expert to coordinate MES and related digital initiatives across production and packaging operations in a GMP/GxP-regulated environment. You will bridge business users, quality, IT, and external partners to ensure compliant system performance.

The role focuses on end-to-end MES coordination, system improvements, and knowledge sharing within the Manufacturing Systems team, contributing to the site’s digital transformation and continuous improvement.

Qualifications

  • Bachelor's or master's degree in engineering, Pharmacy, Chemistry, Biotechnology, Life Sciences, or a related field.
  • Minimum 3 years of experience in production operations, manufacturing systems, or related GMP/GxP-regulated environment.

Responsibilities

  • Coordinate end-to-end MES implementation activities for products and digital initiatives.
  • Identify improvements by analyzing system performance and best practices.
  • Ensure inspection readiness with up-to-date documentation and compliance records.
  • Act as SME for manufacturing systems and promote knowledge sharing within the team.
  • Support design, testing, deployment, and hypercare for system solutions and MBRs.
  • Collaborate with stakeholders to identify needs and drive process optimization and digitalization.
  • Support site digital transformation initiatives and contribute to the digital roadmap.
  • Provide day-to-day operational support and troubleshooting for manufacturing systems.

Skills

Data Analytics
Cross-functional collaboration
GMP knowledge
MES experience

Education

Bachelor's or Master's in Engineering, Pharmacy, Chemistry, Biotechnology, Life Sciences

Tools

MES
SAP
MACO
Seidenader Track & Trace
AGE
Historian
GISC

Job description

Novartis is seeking a Manufacturing Systems Expert to coordinate MES and related digital initiatives across production and packaging operations in a GMP/GxP-regulated environment. You will bridge business users, quality, IT, and external partners to ensure compliant system performance.

The role focuses on end-to-end MES coordination, system improvements, and knowledge sharing within the Manufacturing Systems team, contributing to the site’s digital transformation and continuous improvement.

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