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Lonza

Global life sciences contract manufacturer

Bioprocess Engineer for MMM MC1 DSP

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeVisp, SwitzerlandNo salary listed

About the Job

Requirements

  • A Master's degree in Biotechnology, (Bio)chemical Engineering, Life Sciences, Automation, Industrial Engineering, or a related discipline, or a Bachelor's degree with relevant biopharmaceutical manufacturing experience.
  • Experience in biopharmaceutical manufacturing, with a strong understanding of downstream processing (DSP) processes and good manufacturing practice (GMP) requirements.
  • Knowledge of Manufacturing Execution Systems (MES), electronic Batch Records (eBR), and process automation platforms such as DeltaV.
  • Experience supporting manufacturing operations, troubleshooting process and system-related issues, and driving continuous improvement initiatives.
  • Understanding of data integrity principles, change management, deviation management, and GMP documentation requirements.
  • Excellent communication skills in English.
  • Ability to work in a fast-paced manufacturing environment while maintaining a strong focus on quality, compliance, and operational excellence.

Responsibilities

  • Serve as the Bioprocess Engineer for downstream processing manufacturing operations, ensuring reliable execution of clinical and commercial manufacturing campaigns within safety, quality, and GMP requirements.
  • Act as the primary MES and manufacturing systems representative for the assigned DSP area, supporting recipe execution, troubleshooting, optimization, and continuous improvement activities.
  • Provide first-line support for DeltaV and MES, working closely with Operations, Automation, MSAT, QA, and Technical Support teams to resolve process and system issues.
  • Own, maintain, and review electronic Batch Records, manufacturing recipes, workflows, and associated GMP documentation to ensure compliance, data integrity, and operational efficiency.
  • Lead investigations, deviations, corrective and preventive actions, and change controls related to manufacturing systems, batch execution, and process documentation.
  • Drive digitalization and process improvement initiatives by identifying opportunities to simplify workflows, enhance data visibility, and improve manufacturing performance.
  • Support process transfers, new product introductions, validation activities, and implementation of manufacturing system enhancements.
  • Act as a key interface between Production, Automation, MSAT, QA, and Technical Services to ensure robust and compliant manufacturing operations.

Desired Qualifications

  • German language skills are considered 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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