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Join our Clinical QC Phys-Chem Analytics team in Basel to lead stability programs and quality deliverables supporting innovative biopharmaceutical drug products on a 12-month contract. This is a fully site-based role focused on operational execution across critical customer projects. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

Tasks

  • Manage stability programs and quality compliance for therapeutic drug products.
  • Partner with cross-functional project teams, QA, Sample Management, and global testing laboratories.
  • Coordinate assigned stability studies from initiation through completion, tracking timelines and mitigating operational risks.
  • Author, review, and maintain cGMP documentation including analytical specifications, protocols, and stability summaries.
  • Initiate and progress quality records, supporting deviations, OOX investigations, root-cause analyses, and CAPA resolution.
  • Maintain audit and inspection readiness across all assigned project deliverables and analytical documentation.
  • Develop operational subject-matter expertise across Drug Product analytics to build pathways toward future project leadership.

Requirements

  • Practical experience in a cGMP QC or Analytical Development environment supporting small or large molecule modalities.
  • Technical understanding of physical-chemical analytical techniques (e.g., HPLC, compendial testing) and laboratory data tools (LIMS, Empower, Veeva).
  • Proven track record of authoring GMP documentation and participating in quality event resolution (CAPA, Change Control, OOX, Deviations).
  • Degree or Apprenticeship in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field.
  • Fluent English communication skills with the ability to coordinate across diverse scientific and operational stakeholders.

Benefits

  • An agile career and dynamic working culture.
  • An inclusive and ethical workplace.
  • Competitive hourly rate.
  • Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.
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Über uns
Lonza Group AG ist ein international tätiges Unternehmen für die Pharma-, Biotech- und Life-Science-Industrie. Das Unternehmen entwickelt und produziert Wirkstoffe, biopharmazeutische Produkte sowie spezialisierte Lösungen und unterstützt Kunden von der frühen Entwicklung bis zur industriellen Herstellung. Zudem stellt Lonza chemische und biotechnologische Komponenten für Anwendungen in Gesundheit, Ernährung und weiteren Industrien her.
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