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Lonza

Global life sciences contract manufacturer

Group Leader Drug Linker Development

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

About the Job

Requirements

  • A PhD in Chemistry, Chemical Engineering, or a related discipline is required.
  • Approximately 5–10 years of experience in pharmaceutical process development, API development, clinical supply, or manufacturing sciences is required.
  • Proven experience leading complex projects in a matrix organization within clinical supply, development, or manufacturing operations is required.
  • Strong knowledge of chemical process development, scale-up, technology transfer, and GMP manufacturing requirements is required.
  • Good knowledge of Drug Linker technology and understanding of safe work execution in containment assets is required.
  • People management experience or strong motivation to develop into an expanded leadership role, including coaching and talent development, is required.
  • Demonstrated experience managing project budgets and delivering against performance targets is required.
  • Fluent English language skills are required.

Responsibilities

  • Support the Drug Linker Development Organization Head in ramping up the Accelerate Asset Development unit by defining and supporting implementation of critical business processes for drug linker projects.
  • Manage the hiring process for Accelerate Chemists for the Drug Linker Accelerate Asset with the DL Development leadership team.
  • Lead the assigned Drug Linker Process Development team of Chemists in line with agreed objectives and commitments, and monitor and control their performance.
  • Support the responsible Drug Linker Development Organization Head, in alignment with the Drug Linker Development Teams, in managing and allocating required chemists and laboratory resources.
  • Guide Development and/or MSAT chemists to enable efficient and robust transfer of Drug Linker Processes into supported GMP manufacturing facilities.
  • Drive development and implementation of innovative technologies to increase capability, capacity, and efficiency within Drug Linker Toxin operations, and support laboratory investment programs for introducing relevant technology and tools.
  • Act as a technical and scientific expert for Drug Linker Toxin projects internally and externally, including creating external scientific content to enhance reputation and visibility.
  • Facilitate close collaboration between the Drug Linker Development team and critical interfaces and related product areas such as Bioconjugates and Small Molecules Operations.
  • Lead all human-resources-related aspects for the assigned team and contribute to the scientific development of scientists in their areas of expertise.
  • Ensure compliance with GMP and safety regulations throughout all activities.
  • Support the Head of Drug Linker Organization in assigned initiatives and strategic duties.

Desired Qualifications

  • A PhD in Organic Chemistry is preferred.
  • German proficiency is a strong asset.

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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