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Lonza

Global life sciences contract manufacturer

MES Automation Engineer

Controls & Automation EngineeringPosted on Nov 10
Full-timeVisp, SwitzerlandNo salary listed

About the Job

Requirements

  • A Bachelor's or Master's degree in Automation, Engineering, Biotechnology, Process Engineering, Computer Science, or another relevant technical discipline is required.
  • Experience with industrial automation, process control, or manufacturing systems is required; experience in pharmaceutical or biotechnology manufacturing is ideal.
  • Understanding of working in a GMP-regulated environment, including change control, testing, and documentation, is required.
  • Strong troubleshooting and problem-solving skills, with the ability to systematically investigate automation and production issues, are required.
  • The ability to understand manufacturing processes and translate operational requirements into appropriate automation solutions is required.
  • A structured and well-organized approach, with the ability to manage multiple activities and priorities, is required.
  • Strong collaboration and communication skills, with the ability to work effectively with Manufacturing, Process Engineering, MSAT, QA, IT, and other stakeholders, are required.
  • A solution-oriented mindset and interest in continuous improvement, standardization, and optimization are required.
  • The ability to work independently while contributing effectively within the wider Orca Automation team is required.

Responsibilities

  • Support the DeltaV and MES/Syncade systems within the Orca manufacturing facility to ensure reliable operation and continued support of manufacturing.
  • Develop, modify, and maintain DeltaV and MES recipes, including associated recipe objects and configurations required for production.
  • Implement automation changes through the full lifecycle, including requirements, design, configuration, testing, documentation, and deployment.
  • Support new product introductions and manufacturing campaigns, ensuring required automation and recipe changes are implemented and tested.
  • Create and maintain GMP-compliant automation documentation, including Functional Specifications, Software Test Cases, assessments, and SOPs.
  • Provide automation support for production issues and troubleshooting, working with Manufacturing and other functions to identify root causes and implement sustainable solutions.
  • Support deviations, CAPAs, TCRs, and change controls, including assessment and implementation of required automation actions.
  • Perform and coordinate testing of DeltaV, MES, and associated automation changes before implementation in production.
  • Work with Manufacturing, Process Engineering, MSAT, QA, IT, and other technical teams to translate process and operational requirements into automation solutions.
  • Support standardization and continuous improvement of DeltaV and MES solutions, including the use of standard and reusable automation and recipe objects.
  • Identify and implement improvements to system reliability, operational efficiency, and maintainability.
  • Ensure automation activities comply with applicable GMP, data integrity, quality, safety, and site requirements.
  • Support knowledge sharing, standard ways of working, and continuous improvement within the Orca Automation team.
  • Provide support outside normal working hours in exceptional circumstances when required to minimize impact to manufacturing.

Desired Qualifications

  • Experience with Emerson DeltaV and/or Syncade MES is highly desirable.
  • Experience with recipe development and batch manufacturing systems is an advantage.

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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