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Lonza

Global life sciences contract manufacturer

Manufacturing Science and Technology Process Expert Mammalian Cell Culture DSP

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

About the Job

Requirements

  • A Bachelor's or Master's degree is required; a PhD is preferred.
  • More than 5 years of experience in biopharma manufacturing and/or process development is preferred, preferably in mammalian manufacturing.
  • Knowledge of GMP and a deep understanding of bioprocess technology are required.
  • Fluency in English and German is required.
  • Strong leadership skills are required.
  • Very good communication skills and the ability to interact with customers and the project organization are required.
  • A strong team orientation is required.
  • A structured, focused, and well-organized working attitude is required.
  • Openness to new ideas and suggestions is required.
  • An agile, highly motivated, and dynamic approach is required.
  • A solution-oriented approach is required.

Responsibilities

  • Lead cross-functional teams on technology transfers, including process design, scale-up, and timely process implementation at manufacturing scale; manage assigned projects from planning through coordination, implementation, control, and completion in line with project goals.
  • Act as the interface between process donors, including customers and process development, and operations; ensure process scalability and manufacturability.
  • Apply formal processes and tools to manage information transfer, process-related risks, and change control during technology transfer.
  • Work as an MSAT process expert on capital investment projects for manufacturing-unit construction and commissioning, providing process inputs including block-flow diagrams, media and buffer lists, and critical parameter lists.
  • Implement the manufacturing process in the plant.
  • Interact directly with customers during technology transfer, campaign preparation, execution, and closure, including daily reporting of batch status and performance.
  • Compile process-related deviations, change requests, and campaign reports in a timely manner.
  • Compile CMC sections in filing documents and technical content for validation reports.
  • Contribute to developing and implementing standardized MSAT procedures and processes.
  • Drive continuous improvement of process performance.
  • Supervise tasks in local and global MSAT initiatives or lead major task forces or troubleshooting teams.
  • Evaluate and drive innovative trends within the area of expertise.
  • Mentor scientific and production staff in different areas of expertise.
  • Conduct process-specific training for production staff.
  • Resolve process issues arising during manufacturing while considering regulatory requirements.
  • Execute GMP risk analyses for manufacturing processes.

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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