Alle Stellen
The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. 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 oversee DSP manufacturing campaigns, ensuring execution, monitoring, troubleshooting, and documentation are compliant with cGMP and regulatory requirements.
- Act as the manufacturing Functional Lead for assigned products, coordinating cross-functional teams and maintaining technical expertise in processes, equipment, and facilities.
- Drive risk management activities, including SHE, EM, operational, cleaning, and product risk assessments, while supporting investigations, deviations, CAPAs, and change controls.
- Maintain GMP documentation such as SOPs, manufacturing instructions, risk assessments, and records to ensure compliance and audit readiness.
- Train and support manufacturing personnel, contributing to workforce development and fostering a culture of safety, quality, operational excellence, and continuous improvement.
- Represent manufacturing in capital projects, providing technical input for facility design, equipment selection, commissioning, qualification, and technology transfers.
- Lead continuous improvement initiatives and serve as a manufacturing representative during customer audits, inspections, and strategic cross-functional projects.
- Responsible for the planning, execution, monitoring, and documentation of commercial and clinical manufacturing campaigns within the Downstream Processing (DSP) area.
- Serve as the manufacturing subject matter expert for assigned products, ensuring compliant, safe, efficient, and reliable production according to cGMP requirements, regulatory expectations, and operational excellence standards.
- Support plant operations, lead risk assessments and process improvements, and provide technical expertise for capital projects, commissioning, qualification, and operational readiness.
Requirements
- Strong expertise in biopharmaceutical manufacturing, particularly downstream processing (DSP), with the ability to troubleshoot technical and process-related issues.
- Solid understanding of cGMP requirements and regulatory standards applicable to pharmaceutical manufacturing.
- Experience managing quality systems and compliance activities, including risk assessments, deviations, CAPAs, change controls, and validation.
- Proven problem-solving skills with the ability to identify root causes and implement effective corrective actions.
- Strong communication and stakeholder management capabilities, enabling effective collaboration across functions and organizational levels.
- Demonstrated project leadership and team coordination experience within complex, regulated manufacturing environments.
- Bachelor's or Master's degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences, or a related field, along with relevant experience in biopharmaceutical manufacturing, process engineering, technical operations, or cGMP-regulated environments.
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, 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.