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Lonza

Global life sciences contract manufacturer

Biotechnologist Drug Product

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

About the Job

Requirements

  • Several years of experience in a GMP shop-floor environment, preferably in sterile Drug Product manufacturing.
  • Fluency in English is required.
  • Familiarity with GMP requirements, quality procedures, and standard operating procedure execution is required.
  • Preparedness to work a three-shift pattern, including nights and Saturdays, is required.

Responsibilities

  • Execute manufacturing activities in the Drug Product area.
  • Ensure batch execution according to current Good Manufacturing Practice guidelines, evaluate test results, resolve issues, troubleshoot manufacturing equipment, and recommend resolutions.
  • Provide front-line technical and procedural support while working with the manufacturing team.
  • Ensure each batch is manufactured safely, on time, and in compliance with batch instructions and quality requirements.
  • Prepare, execute, and review batch records and other relevant GMP documents for the assigned production area in a timely manner and to a high standard.
  • Support process-related investigations and assist in decision-making on production issues.
  • Support process changes and corrective and preventive actions related to processes within required timelines.
  • Perform training activities in relevant areas as an operator and support colleagues and new joiners.
  • Operate, set up, and clean production equipment and premises for liquid and freeze-dried drug forms, including compounding, parts washing, autoclaving, filter integrity testing, and visual inspection.

Desired Qualifications

  • German language skills are a plus.
  • IT knowledge, including knowledge of SAP and manufacturing execution systems, is beneficial.

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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