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The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Join a collaborative, proactive and diverse team where you will drive process excellence across compounding operations, support operators with technical expertise, lead deviations, investigations, and execute validation and qualification activities while ensuring continuous inspection readiness. As part of an exciting greenfield growth project, you will take ownership, make a visible impact, and contribute to the successful delivery of safe, high-quality products. This is a fully site‑based role. 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

  • Lead and continuously improve aseptic compounding processes, leveraging GMP manufacturing experience to ensure safe, compliant, and efficient operations.
  • Provide hands-on technical support to operators, troubleshoot process issues, and drive deviations, investigations, and corrective actions to maintain product quality and compliance.
  • Execute and support validation and qualification activities, including the preparation, review, and maintenance of all relevant GMP documentation.
  • Maintain equipment and processes in an inspection-ready state, support internal and external audits, and contribute expertise in sterile manufacturing environments.

Requirements

  • Bachelor’s or Master’s degree in a Life Sciences discipline (e.g., Biotechnology, Pharmacy, Biology, Chemistry) with hands-on experience in aseptic/sterile manufacturing environments.
  • Proven experience in GMP-regulated manufacturing, with a strong understanding of quality, compliance, and documentation requirements is a must.
  • Experience in qualification and validation activities are a strong advantage.
  • Fluent English and conversational German (B1 level or above), enabling effective communication across teams and functions.
  • A proactive, reliable team player who enjoys collaborating with others, takes ownership of responsibilities, and thrives in a fast-paced environment with changing priorities and multiple parallel activities.
  • Comfortable navigating ambiguity with a high degree of flexibility; experience in thawing and compounding operations and knowledge of GMP washers and autoclaves are considered strong advantages.

Benefits

  • An agile career and a dynamic work culture.
  • An inclusive and ethical workplace.
  • Compensation programs that recognize high performance.
  • In addition to a competitive salary, you can expect numerous 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.
Das Team

Collaborate within a proactive, reliable, and accountable team.

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