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CSL

Develops and delivers biotherapies and vaccines

Senior Automation Engineer PCS/MES

Bioprocess & BiomanufacturingUpdated on Nov 15
Full-timeBern, SwitzerlandNo salary listed

About the Job

Requirements

  • Bachelor's or master's degree in Automation, Electrical Engineering, Computer Science, Process Engineering, or a comparable qualification.
  • At least 5 years of professional experience in automation and MES in a GMP-regulated environment, preferably in the pharmaceutical industry.
  • Strong knowledge of Siemens PCS 7 and Batch.
  • Strong knowledge of Siemens Opcenter Execution Pharma.
  • Experience with pharmaceutical manufacturing processes, ideally aseptic filling.
  • Strong knowledge of GMP requirements and experience with CSV, Data Integrity, Annex 11, and GAMP 5.
  • Knowledge of ISA-S88 and ISA-S95 standards.
  • Experience leading technical projects and collaborating with interdisciplinary teams.
  • Strong analytical abilities and a structured, independent working style.
  • Very good spoken and written German and English.

Responsibilities

  • Ensure reliable production in aseptic and GMP-regulated filling facilities.
  • Operate, develop, and provide lifecycle support for automation and Manufacturing Execution Systems in the Filling area.
  • Realize investment projects and coordinate and implement changes for process optimization, compliance assurance, and troubleshooting on complex production systems.
  • Lead automation and MES projects as an automation/MES subproject lead.
  • Specify, implement, commission, qualify, and provide lifecycle support for PCS 7, SIMATIC Batch, and Opcenter systems.
  • Create, maintain, and optimize electronic Manufacturing Batch Records and batch processes according to ISA-S88 and ISA-S95.
  • Configure and develop Siemens Opcenter Execution Pharma (MES), including interfaces to SAP, LIMS, Data Historian, and Package Unit systems.
  • Analyze and resolve complex production disruptions and conduct root-cause analyses.
  • Support GMP-related activities, including CAPAs, deviations, change controls, and inspections.
  • Create and review GMP documentation, specifications, risk analyses, test documents, and qualification documents.
  • Support FAT, SAT, commissioning, IQ/OQ/PQ, and CSV activities.
  • Ensure reliable operation of production and automation systems.
  • Implement process improvements and digitalization initiatives to increase efficiency, quality, and equipment availability.
  • Manage and coordinate external integrators and suppliers.

Desired Qualifications

  • Professional experience in a GMP-regulated environment, preferably in the pharmaceutical industry.
  • Experience with pharmaceutical manufacturing processes, ideally in aseptic filling.

About the Company

CSL

Develops and delivers biotherapies and vaccines

CSL is a global biotechnology company that develops and delivers biotherapies and influenza vaccines. It focuses on plasma-derived and recombinant therapies for rare and serious diseases and sells to healthcare providers, hospitals, and governments across the Americas, Asia Pacific, and Europe. Its product range includes treatments for rare diseases, influenza vaccines, and antivenoms, produced through its R&D, manufacturing, and distribution operations. CSL differentiates itself by offering the broadest portfolio of plasma-derived and recombinant therapies and by leveraging its global footprint and emphasis on diversity to reach diverse markets. The company’s main goal is to save lives and protect health by expanding access to high-quality therapies and vaccines worldwide.

Company size
10,001+
Company stage
IPO
Headquarters
Parkville, Australia
Founded
1916

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