Position: Mid-Senior level

Job type: Full-time

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Job content

My main tasks will be...
  • Support the definition of manufacturing process from the beginning
  • Operating the production processes and related equipment according to GMP, GDP, and safety guidelines.
  • Carrying out cleaning and support maintenance activities
  • Monitoring and follow-up the production processes and alarming according to the operating instructions
  • Recognizing, interpreting and eliminating malfunctions and deviations
  • Independent performance of on-site analyses
  • Documenting and maintaining according to GMP and GDP production records
  • Actively participation in Huddle/Hoshin Level 0 meeting
I bring with me...
  • Completed basic technical training as a chemical technician, machine mechanic or similar
  • More than 5 years of professional experience in a GMP-regulated production plant or career starter after completed training
  • Very good knowledge of written and spoken English
  • Good GMP knowledge
  • Drive for continues improvement and act proactively
  • Independent, agile, flexible, accurate and clean way of working
  • Willingness to work in a 2-model shift pattern
My reasons for choosing Bacthera...
  • Innovative and fast growing start-up company with short decision-making processes
  • Motivated, agile and multinational team
  • Fringe benefits (e.g. Lunch card, deduction at different stores (such as Adidas, Samsung), allowance for public transport)
  • Interesting and diversified tasks
My future working place will be...Visp, SwitzerlandAbout UsBacthera is a leading contract development and manufacturing partner (CDMO) for biotech and pharma customers. We enable our customers to bring life-changing treatments to patients. We operate from our headquarters in Basel (CH) and have production facilities in Denmark and Switzerland. We bring together best-in-class, complementary capabilities and we are the first CDMO globally to provide a full supply chain that offers manufacturing of live bacteria strains for therapeutic use.
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Deadline: 18-05-2024

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