Principal Scientist, Bioanalytics - Drug Development Lead

Lonza; Basel; Sur place; Vertraulich; Plein temps

Avantages offerts par ce poste

Agile culture

Inclusive workplace

Performance-based compensation

Résumé du poste

Lonza in Basel is seeking an Associate to Principal Scientist Bioanalytics to lead pharmaceutical development projects across pre-clinical stages. You will ensure delivery of work packages, generate reporting data, and drive quality through robust analytical testing, including method transfer and investigations.

The role requires a PhD and 2–3 years of industry experience with potency assays, strong knowledge of cell-based assays, ELISA, enzyme assays, and SPR.

Qualifications

• PhD or equivalent in Biochemistry, Biotechnology, Analytical Science, or related Life Sciences.
• 2–3 years industrial experience in Life Sciences as a research or technical expert.
• Experience with potency assays for modalities (e.g., mAbs, Bi/trispecifics, enzymes, peptides, recombinant proteins, ADCs).

Responsabilités

• Lead and manage pharmaceutical development projects in Development Bioanalytics (DevBA) from customers and pre-clinical stages.
• Accountable for on-time delivery of work packages, provision of analytical testing results, documents and reports.
• Proactively address risks and resolve issues with clear communication to all stakeholders.
• Represent DevBA in Lonza internal and customer meetings as SME.
• Support stakeholders to maintain planning tools.

Connaissances

Cell-based assays

Analytical techniques

Excellent communication

English fluency

Formation

PhD in Biochemistry / Analytical Science / Life Sciences

Outils

ICH Q14 / Q2 guidelines

Description du poste

Lonza in Basel is seeking an Associate to Principal Scientist Bioanalytics to lead pharmaceutical development projects across pre-clinical stages. You will ensure delivery of work packages, generate reporting data, and drive quality through robust analytical testing, including method transfer and investigations.

The role requires a PhD and 2–3 years of industry experience with potency assays, strong knowledge of cell-based assays, ELISA, enzyme assays, and SPR.