03.07.25 | Vollzeit | Bern | Michael Page InternationalUpstream processing of mammalian cell culture, working in shifts. The assignment will be temporary for the next 12 months, to start as soon as possible
Später ansehen27.06.25 | Teilzeit | Bern | Schneider Electric GmbHWorking student in Business Intelligence/ Data analytics (f/m/d) What? Working student in Business Intelligence (f/m/d) for 40-50% (16-20 h/week). Where? Gümlingen (Bern) or Crissier, Switzerland When? 01.01.2025 for at least 12 months. Who is looking for your support? Jürgen Lieber, Business
Später ansehen23.06.25 | Vollzeit | Bern | jobwinner.chConsultation regarding new infrastructure projects. - We provide you with enough freedom to create and tackle new challenges, working together with a highly motivated
Später ansehen12.06.25 | Vollzeit | Bern | Michael Page InternationalBiotechnology company in Solothurn, we are currently looking for several experienced Manufacturing Associates - different levels of experience - for automated upstream processing of mammalian cell culture, working in shifts. The assignment will be temporary for the next 12 months, to start as soon as possible
Später ansehen02.05.25 | Vollzeit | Bern | Oxford Global ResourcesProduction processes, supporting investigations of deviations, and helping implement corrective actions to uphold GMP standards. You will also contribute to training initiatives and internal audit preparation. Strong documentation skills and a detail-oriented approach are essential to success in this role
Später ansehen02.05.25 | Vollzeit | Bern | Oxford Global ResourcesProduction processes, supporting investigations of deviations, and helping implement corrective actions to uphold GMP standards. You will also contribute to training initiatives and internal audit preparation. Strong documentation skills and a detail-oriented approach are essential to success in this role
Später ansehen31.10.19 | Vollzeit | Bern | DecomplixYou bring - a technical background and enjoy writing technical documents; - professional experience in quality management or regulatory affairs in the Medtech industry; - detailed knowledge of ISO 13485 and the certification processes for medical devices in Europe, ideally for software-only products
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