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This role is important for ensuring successful technology transfers, maintaining GMP compliance, and driving continuous improvement. If you're a proactive problem-solver with a strong background in manufacturing science and technology, this position based in Visp, Switzerland, offers relocation for successful candidates and their families if needed.

Tasks

  • Implement the manufacturing process in the plant as received from DP process development or customer.
  • Secure success during technology transfer by applying formal processes and tools to handle the transfer of information, process-related risks, and change control.
  • Participate in GMP risk analysis for manufacturing processes.
  • Communicate manufacturing updates to the customer.
  • Lead and/or participate in cross-functional teams as an MSAT guide tasked with technology transfers (process implementation and transfer) and timely process implementation at manufacturing scale, including the whole lifecycle of assigned projects from planning, coordination, implementation, control, and project completion aligned with project management goals.
  • Lead or participate in change controls and deviation investigations.
  • Prepare and perform Qualification and Validation activities in compliance with cGMP regulations and specification requirements.
  • Contribute to the development and implementation of standardized MSAT procedures and processes.
  • Responsible for continuous improvement of process performance and product quality.
  • Proactively anticipate, evaluate, and resolve scientific and technical challenges within area of expertise.
  • Act as a mentor for scientific and production staff in different fields of expertise.
  • Act as a link between Drug Product Services (DPS Basel), mainly formulation, process development and manufacturing, QC and Visp.
  • Look after process monitoring and process control strategy as well as sophisticated data analysis.

Requirements

  • Degree in Pharmaceutical Technology, Biotechnology, Chemistry, Process Engineering or equivalent scientific degree.
  • More than 3 years of proven track record in the area of sterile manufacturing on the shopfloor and/or MSAT, QA/QC.
  • Proficiency in English.
  • Proven process understanding in sterile manufacturing (Pharma, Regulatory aspects, freeze-drying).
  • Very good interpersonal skills with all kinds of interfaces within customers and the project organization.
  • Strong team orientation and collaboration across groups within a matrix organization.
  • Structured, focused and well-organized working demeanor.
  • Open-minded for new insights and suggestions.
  • Agile, highly motivated and dynamic drive.
  • Driven to resolve issues.

Benefits

Relocation is available for a successful candidate and their family, if needed.

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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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