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Lonza

Project Coordinator Bioconjugates Research

24 March 2026

Full-Time Netherlands

Department

Health & Biotech

Job Category

Health & Biotech

Description

  • Maintain a strong connection to bioconjugation science in multiple different indications by applying relevant expertise, interpreting project data (generated by LONZA internal teams, external partners, CROs and CMOs), using insights originating from multiple different sources (scientific publications, patents, specific databases) to guide opportunity identification, the ideation process, problem‑solving and, and providing well‑reasoned input to support project and organizational decision‑making.
  • Own project plans, stage‑gate readiness packages including compilation of briefing documents, and stage decision; ensure data‑driven progression through stage-gates up to launch activities.
  • Manage and track budgets against plan, deadlines, allocate resources, and external spend (e.g., CRO/CMO) in line with project priorities inform Head of R&D Bioconjugates Research (Oss).
  • Prepare business case / NPV assessments, launch/soft launch local.
  • Maintain a strong overview across programs, projects, workstreams, monitor risks, engage in scenario planning, and delineate critical path activities.
  • Will have a dotted line to the Head of R&D Portfolio management working closely on governance, best practice, information sharing, etc., as part of wider Lonza R&D community
  • Contribute to the portfolio overview and prioritization; surface interdependencies and escalate bottlenecks to the Head of R&D Bioconjugates Research (Oss).
  • Prepare and present concise, decision‑ready updates (e.g., for stage‑gate reviews, governance forums, partner meetings);
  • Demonstrate organizational agility and is able to connect internal and external partners, fostering an atmosphere of collaboration and further integration within the global R&D organization;
  • Gain data regarding competitors’ activities.
  • Communicate professionally in English (written and verbal) and take care of stakeholders across scientific, operational, and executive audiences.

Qualifications

  • MSc degree in Biochemistry, Drug Discovery, Molecular Life Sciences, Medicinal Chemistry or related field.
  • Master with 1 0 years relevant experience, or PhD with 5 years of relevant experience in Biotech/pharma/CDMO/CRO
  • Background in ADC, bioconjugation, antibodies, small molecules/ payloads
  • Broad understanding of biological processes/ pathways and indication areas (immunology, neurodegeneration, oncology)
  • Scientific expertise with critically analyzing data sets and results, with pragmatic problem‑solving
  • Project leadership: planning, risk/issue management, stage‑gate readiness, and transparent decision‑making.
  • Influence & communication: clear storytelling and stakeholder alignment
  • Organizational agility: able to be the connective hub across internal and external partners.
  • Data‑driven mindset: uses literature, internal data, and benchmarks to guide choices.
  • Proficiency with project tools (e.g., Smartsheet, MS Project, or similar).
  • There is no visa sponsorship available for this role.

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