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Lonza

Global life sciences contract manufacturer

EI&C MES DeltaV Application Manager

Enterprise ApplicationsConfirmed live in the last 24 hours
Full-timeVisp, SwitzerlandNo salary listed

About the Job

Requirements

  • A completed university degree in Computer Science, Industrial IT/OT, Automation Engineering, or a related field at Bachelor's level or higher is required.
  • Significant professional experience in IT/OT, MES DeltaV (formerly Syncade), or automation-related engineering roles within a regulated environment is required.
  • A solid understanding of GMP requirements and experience working with validated production or automation systems are required.
  • Responsibility for the MES lifecycle, including system operation, enhancements, release management, and interface coordination, is required.
  • Strong knowledge of OT networks, virtualization technologies such as VMware, system architectures, and basic cybersecurity principles is required.
  • Fluency in German or English at a minimum B2 level is required for effective collaboration with local and global stakeholders.
  • A structured and independent working style, strong communication skills, and problem-solving skills are required.
  • Willingness to participate in on-call duty two to three times per year is required.

Responsibilities

  • Execute and lead MES DeltaV projects across all lifecycle phases, including requirement analysis, design, implementation, testing, and deployment.
  • Maintain, optimize, and further develop MES standards, ensuring consistency, compliance, and alignment with site and global guidelines.
  • Ensure reliable operation, enhancement, and updating of MES DeltaV (formerly Syncade) systems, recognizing their direct impact on production processes and GMP-compliant documentation.
  • Collaborate closely with Operations, QA, Automation, and IT/OT teams to ensure seamless system integration and high system availability.
  • Analyze and improve MES-related workflows, identifying opportunities for digitalization, efficiency gains, and data integrity improvements.
  • Coordinate and manage external partners and vendors involved in MES or OT-related project and support activities.
  • Ensure GMP-compliant execution of all MES and OT activities, including documentation, change control, and validation readiness.

About the Company

Lonza

Global life sciences contract manufacturer

Lonza is a global provider of development and manufacturing services for the pharmaceutical, biotechnology, and nutrition sectors. It supports clients from early development through to commercial production, offering integrated processes such as process development, GMP manufacturing, formulation, fill-finish, and quality assurance to bring medicines and nutrition products to market. Lonza’s model is built on end-to-end CDMO capabilities, enabling companies to move from concept to scalable, compliant production with reliable supply chains. What sets Lonza apart is its long history and global footprint, combining decades of experience across chemistry, biology, and nutrition with a broad, end-to-end service network that supports projects from discovery to commercialization. The company aims to be a trusted, long-term partner in life sciences by helping customers efficiently develop and manufacture their products at scale while maintaining strict regulatory and quality standards.

Company size
10,001+
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1897

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