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This position is based in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families. As GMP Compliance & Quality Improvement Lead, you will help strengthen quality and compliance across the Quality Control (QC) organization by identifying compliance gaps, guiding investigations, and leading improvements to support reliable laboratory processes. You will share your expertise and help teams prepare for regulatory inspections.

Tasks

  • Assess QC processes against Good Manufacturing Practice (GMP) requirements, identify compliance risks, and implement lasting improvements.
  • Translate regulatory requirements into practical guidance on laboratory processes, data integrity, and documentation.
  • Support inspection readiness and regulatory inspections, advising QC teams on compliance questions.
  • Lead and write deviation investigations, identify root causes, and develop effective corrective and preventive actions (CAPAs).
  • Review and approve compliance documentation and quality records to ensure they meet regulatory expectations.
  • Lead improvement projects with QC, Quality Assurance, Manufacturing, and Technical Operations, using quality metrics and trends to address recurring issues.
  • Coach colleagues on GMP, quality risk management, and inspection readiness, encouraging shared responsibility for quality.

Requirements

  • A master’s or doctoral degree in life sciences, chemistry, pharmacy, biotechnology, or a related field; or a bachelor’s degree with extensive relevant experience.
  • At least two to three years of experience in a GMP-regulated pharmaceutical or biotechnology environment.
  • Practical knowledge of Swissmedic, FDA, and EU GMP requirements, EMA expectations, ICH guidelines, and the US and European Pharmacopoeias.
  • Experience working with regulatory authorities and supporting inspections.
  • Extensive experience writing and leading deviation investigations, identifying root causes, and developing CAPAs.
  • Experience identifying compliance gaps, applying quality risk management, and leading improvement projects across teams.
  • Clear technical writing, analytical, and communication skills, with the ability to build agreement, constructively question processes, and independently complete initiatives.
  • Clear communication skills in English with a collaborative working style.
  • German language is an advantage.

Benefits

  • Opportunities to develop your career and lead meaningful quality improvements.
  • An inclusive and ethical workplace where your ideas are valued.
  • A competitive salary and compensation programs that recognize high performance.
  • A range of lifestyle, family, and leisure benefits.
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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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