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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.

The MSAT Process Specialist of DSP at Lonza AG will play a key role in supporting the successful transfer, scale-up, validation activities, and continuous improvement of biopharmaceutical manufacturing processes. This individual will provide technical expertise and hands-on support to ensure robust and efficient production.

Tasks

  • Execute and oversee process validation activities in downstream unit operations.
  • Support the transfer of new manufacturing processes from R&D to manufacturing, ensuring successful scale-up and validation activities.
  • Support root cause analysis for process deviations and implement effective corrective and preventive actions (CAPAs).
  • Develop and revise process documentation, including process description, validation protocols and reports, standard operating procedures (SOPs), and technical reports.
  • Provide technical support to manufacturing operations for troubleshooting and continuous process improvement initiatives.
  • Collaborate with cross-functional teams including Manufacturing, Quality, Engineering, and R&D.
  • Support regulatory submissions.
  • Conduct data analysis and trending to monitor process performance and identify areas for improvement.

Requirements

  • Bachelor's or Master's degree in Chemical Engineering, Biotechnology, Biochemistry, or a related scientific discipline.
  • Minimum of 3-5 years of experience in process development, MSAT, or manufacturing support within the biopharmaceutical industry.
  • Strong understanding of downstream (purification) manufacturing processes.
  • Experience with process scale-up, technology transfer, and validation activities.
  • Proficiency in data analysis and statistical tools.
  • Excellent problem-solving skills and a strong analytical mindset.
  • Ability to work effectively in a fast-paced, team-oriented environment.
  • Strong written and verbal communication skills in English.
  • Knowledge of cGMP regulations and quality systems.

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.
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