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Lonza

Global life sciences contract manufacturer

Laboratory Coordinator HAPI Laboratory

Regulatory & Quality (Life Sciences)Posted on Nov 13
Full-timeVisp, SwitzerlandNo salary listed

About the Job

Requirements

  • Completed training as a laboratory technician or comparable education in a natural-science field.
  • Several years of practical experience in a synthesis or development laboratory.
  • Experience handling highly potent active substances in a GxP-regulated environment.
  • Knowledge of SOP management and a good understanding of GMP requirements.
  • Strong practical knowledge of laboratory equipment.
  • Ability to work independently, in a structured and responsible manner, with a strong quality focus.
  • Very good German language skills.
  • Strong teamwork and communication abilities.

Responsibilities

  • Coordinate and support laboratory processes, SOPs, risk assessments, training, and laboratory and installation projects in the HAPI Laboratory E38.
  • Ensure laboratory operational readiness and coordinate maintenance, housekeeping, logistics, ordering activities, and recommissioning after operational disruptions.
  • Maintain the laboratory's GMP qualification status and support compliance with regulatory requirements and technical adaptations.
  • Contribute to laboratory planning and the continuous optimization of laboratory systems, workflows, and containment concepts.
  • Support IT and CSV qualification activities for laboratory systems and equipment.
  • Contribute to the setup, installation, and operation of the Drug Linker laboratory as part of the Accelerate project in H08.
  • Take coordinating or leading roles in technical laboratory projects and support cross-functional Drug Linker activities in E38 and E52.

Desired Qualifications

  • IT and CSV experience.
  • English language skills.

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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