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A leading cloud IT infrastructure and service provider with offices in Basel and Zürich, Switzerland is looking for a Systems Engineer with Project Management experience. Would you like to help setup big data or Kubernetes platforms and help customers to get their infrastructure up and running on these platforms? Do you like a mixture of hard core technology along with taking responsibility to deliver projects and handle the communications with customers? We are looking for candidates with experience in or excellent familiarity with Openstack, Kubernetes, Apache Sparc, Hadoop, Casandra, Openshift, Docker, VMware/vCloud and KVM as well as commercial public cloud systems. Skills in the open source world (Linux, MySQL/MariaDB, Postgres, Python etc.) as well as in the Microsoft world (Windows server, MS SQL, Exchange etc.) should be part of candidates standard repertoire. Basic networking skills are a must have. We expect 5 years of relevant IT work experience for this position. About Safe Swiss Cloud: We are a leading Swiss cloud infrastructure provider with our own data centres and operate a number of cloud platforms for big data, ERP and other enterprise solutions. Our customer base is international and is mostly in the areas of Software, Finance/Banking/Insurance, Pharma etc. Fluent spoken and written English is essential. German and/or French are an advantage. Please contact us at (see below) Work permit for Switzerland or the EU is required. No agencies please.

A leading cloud IT infrastructure and service provider with offices in Basel and Zürich, Switzerland is looking for a Systems Engineer with Networking experience. Would you like to help setup big data or Kubernetes platforms and help customers to get their infrastructure up and running on these platforms? Do you like a mixture of technology, operations and support? We are looking for candidates with experience in or excellent familiarity with Openstack, Kubernetes, Apache Sparc, Hadoop, Casandra, Openshift, Docker, VMware/vCloud and KVM as well as commercial public cloud systems. Skills in the open source world (Linux, MySQL/MariaDB, Postgres, Python etc.) as well as in the Microsoft world (Windows server, MS SQL, Exchange etc.) should be part of candidates standard repertoire. Basic networking skills are a must have. We expect 3+ years of relevant IT work experience for this position. About Safe Swiss Cloud We are a leading Swiss cloud infrastructure provider with our own data centres and operate a number of cloud platforms for big data, ERP and other enterprise solutions. Our customer base is international and is mostly in the areas of Software, Finance/Banking/Insurance, Pharma etc. Fluent spoken and written English is essential. German and/or French are an advantage. Work permit for Switzerland or the EU is required. No agencies please.

At Roche, over 90,000 people across 150 countries are pushing back the frontiers of healthcare. Working together, we've become one of the world's leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity. In Product Development Medical Affairs, PHC (Personalized Healthcare) and Patient Access, we translate personalized healthcare into better..... click apply for full job details

Junior Scientist - innovative cell models for drug testing Basel Roche Pharma Research and Early Development (pRED) translates extraordinary science into medical innovation through a diversity of technologies and talent located across seven research sites worldwide. We deliver on individual patient needs through a deep understanding of disease biology and the implementation of Personalized Healthcare strategies. We provide in vitro safety and Absorption, Distribution, Metabolism, and Excretion (ADME) data packages that allow selection of best drug candidates while enabling lean and fast development. We establish innovative tailor made solutions to address human relevance of safety flags, support clinical dose selection and provide compliant data packages for clear decision making and regulatory filing. We integrate cutting edge science to deliver fast and predictive ADME & Safety solutions for Pharma Research and Early Development (pRED). Our collaborative spirit and ad-hocracy mindset allows for tailored, human-relevant solutions using advanced cellular models. We provide translational approaches bridging human cells to patients. About Us We believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about transforming patients' lives. We are courageous in both decision and action. And we believe that good business means a better world. That is why we come to work each day. We commit ourselves to scientific rigour, unassailable ethics, and access to medical innovations for all. We do this today to build a better tomorrow. We are proud of who we are, what we do, and how we do it. We are many, working as one across functions, across companies, and across the world. We are Roche. Activities and responsibilities You think "just contributing" is not enough? You would like to pave the way how we do drug safety assessment in future? We are seeking a highly motivated scientist dedicated to the development and application of advanced human cellular models such as 3D cell culture, organ-on-a-chip and microphysiological systems to support the safety assessment of small and large molecule drug candidates. You will be part of a team of skilled and dedicated scientists, developing and implementing new approaches towards improved in vitro safety assessments of new drugs. You will innovate, develop and apply state-of-the-art cellular models and most modern imaging readouts to improve and accelerate human relevant safety assessment while reducing animal use. By this you will directly impact pre-clinical and clinical research with your expertise in cellular biology, complex cellular in vitro models and imaging. The candidate: Ph.D. degree in cell biology, bioengineering or related fields. Significant experience with human cell culture, ideally including stem-cells (iPS), 3D models, microphysiological systems and organ-on-a-chip technologies. Excellent skills in immunostaining, confocal imaging and quantitative image analysis. Good understanding of neuroscience and molecular biology is highly desired. Independent research skills such as designing, executing and interpreting experiments, as demonstrated by previous publications. Documenting, reporting and presentation of research results in internal and external meetings Exceptional communication skills, strong passion and dedication to science and work well within a group.

General information: - Start date: 10.06.2019 - Latest start date: 17.06.2019 - End date: 31.12.2019 - Extension: Might be possible, needs to be approved (phase 2 planned for 2020). - Workload: 100% - Remote/Home Office: Not preferred at the beginning, later possible (up to 1 day per week). - Travelling: Only between Basel and Kaiseraugst. Tasks & Responsibilities: - The experienced resource will collaborate with the Project Manager, Project Business Lead and Stakeholders to establish drive successful change. - Organizational Change Management planning and execution - Communications planning and execution, including preparation of materials. *What are the key technical skills that all candidates must attain? Must Haves: - Minimum 5 years of experience in change management and communications (Prosci highly desired) - Minimum 5 years of experience in complex project environment - Very good command of business English - Business-minded and proactive way of working *What desirables skills would be useful for candidates to possess that can add value towards the project? Nice to Haves: +++ Experience in software implementation and/or chance is an advantage +++ Experience with HR and Procurement topics is an advantage +++ German highly appreciated

Als unabhängiges Familienunternehmen entwickeln und gestalten wir zukünftige Lebensräume. Mit gemeinsamem Wissen und Ihrer Leidenschaft schaffen wir im Team wegweisende Lösungen. Wir sind eine führende Schweizer Planungs- und Beratungsgruppe mit rund 450 Mitarbeiterinnen und Mitarbeitern. Innerhalb der Rapp Gruppe planen die Spezialisten/-innen der Rapp Gebäudetechnik AG integrale..... klicken sie bewerben, für die volle Stellenbeschreibung

Unser Auftraggeber ist eine selbständig CH-Firma im Raum Basel. Das Unternehmen ist weltweit aktiv und in den wichtigsten Absatzländern bei den Heilmittelbehörden registriert. Der Lohnbetrieb fertigt Feststoffe wie Tabletten, Kapseln etc. Von klassischen Film-/ Brausetabletten über retardierende Produkte bis Multi-Unit-Pellet-Systemen in höchster Qualität. Zwei unabhängige Bulk-Produktionslinien..... klicken sie bewerben, für die volle Stellenbeschreibung

Die Celonic AG ist ein international tätiges und schnell wachsendes Dienstleistungsunternehmen im Bereich der Biotechnologie. Als CDMO bieten wir Services zur Produktion von Biopharmazeutika an, beginnend bei der Zelllinienentwicklung bis zur GMP-gerechten Herstellung von therapeutischen Proteinen für klinische Phasen und die Marktversorgung. Wir sind empathisch, effizient und..... klicken sie bewerben, für die volle Stellenbeschreibung

Du suchst einen Arbeitgeber, der genau zu Dir passt? Uns ist es wichtig, dass Du Dich bei uns von Anfang an wohlfühlst. Deshalb lassen wir Dich in Deiner Ausbildung auch nie allein: Dein Ausbilder, die Kollegen und Azubis der höheren Lehrjahre helfen Dir es besser zu machen und unterstützen Dich auf dem Weg zum erfolgreichen Abschluss. Deine Aufgaben:..... klicken sie bewerben, für die volle Stellenbeschreibung

Du suchst einen Arbeitgeber, der genau zu Dir passt? Uns ist es wichtig, dass Du Dich bei uns von Anfang an wohlfühlst. Deshalb lassen wir Dich in Deiner Ausbildung auch nie allein: Dein Ausbilder, die Kollegen und Azubis der höheren Lehrjahre helfen Dir es besser zu machen und unterstützen Dich auf dem Weg zum erfolgreichen Abschluss. Du bist handwerklich geschickt und willst Heavy Metal zu..... klicken sie bewerben, für die volle Stellenbeschreibung

Celonic AG is an internationally operating, rapidly growing service provider for the biotech industry. As a Contract Development and Manufacturing Organization (CDMO) we provide a broad portfolio of services to our global customers, ranging from Cell Line Development all the way up to GMP Manufacturing. We are empathic , efficient , and excellent . To us, this means that: We attentively listen to each other, our customers and our business partners, in order to obtain the best understanding of their exact needs or problems. We are transparent and flexible in our communication and our working processes, with a focus to always find the resource optimized way to the best solution. We always strive to be the best by far in every competitive environment. This philosophy applies to our products, our services, our behavior towards our customers and partners. For support of our USP Team at our Basel site (Switzerland) we are looking for Director (f/m/d) Upstream Processing (USP) Process Development Job description: Leading the complete USP Team responsible for Process Development Prove leadership for developing next-generation USP bio-solutions portfolio and platforms, including high throughput process development Actively support the yearly budgeting process for growth investments Providing in-depth upstream processing expertise to the team and actively engaging in trouble shooting activities Organizing asset and personnel resources Representing the USP Team in client meetings Supporting Sales and Project Management in realizing new customer projects Working on internal projects for continuously improving USP development strategy Reporting to the Vice President Biopharmaceutical Development Qualification and skills: Master or PhD in Biotechnology, Biochemistry or Biology Minimum 10 years experience with cultivation of mammalian cells Minimum 7 years industry experience in USP process development of biopharmaceuticals, GMP production experience favorable Proven capabilities in leading employees Experience with single-use bioreactors from mL-scale to 2000 L production scale, experience with automated multi-parallel bioreactors favorable Experiences in performance of process characterization and process validation favorable Vast experience with mammalian cell cultures (e.g. CHO, HEK and human cell lines) and thorough knowledge of cultivation techniques Empathic and solution oriented personality with sound communication skills and proven leadership experience Proven capabilities in working in interdisciplinary teams Excellent English skills, German skills favorable Our offer: Permanent employment Flexible working hours Corporate Fitness program Personal development based on individual capabilities Broad insight in various areas of development and manufacturing Corporate culture build on recognition, respect and empathy

Celonic AG is an internationally operating, rapidly growing service provider for the biotech industry. As a Contract Development and Manufacturing Organization (CDMO) we provide a broad portfolio of services to our global customers, ranging from Cell Line Development all the way up to GMP Manufacturing. We are empathic, efficient, and excellent. To us..... click apply for full job details

Clinical Study Disclosure Manager - Basel-Land Jocelyn Blackham is recruiting for a Clinical Study Disclosure Manager to join a rapidly growing drug discovery company at their site based in Basel-Land on a contract basis for 12 months, with the possibility of extension. The main purpose of the role will be to: - Lead, execute and manage current and future clinical trial disclosure and transparency activities. - Drive the processes for clinical study protocol registration and summary results posting on public clinical trial registries. - Ensure accuracy, consistency, quality, and compliance of publicly disclosed clinical trial information, in accordance with applicable global clinical transparency regulations and company policy and processes. - Work with study and/or project teams (e.g., Therapeutic Area, Clinical operations, Biostatistics, Regulatory Affairs, Life Cycle Management, Patent and Legal) to plan and execute study disclosure activities. Further responsibilities will include: - Serve as a subject matter expert, advise on evolving global clinical trial disclosure and transparency laws, regulations, and requirements, and provide guidance on best practices. - Provide leadership for transparency initiatives such as lay language results summaries or clinical data sharing. - Proactively identify opportunities to improve systems and processes and lead process improvement initiatives for disclosure/transparency. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - Preferably, a higher degree in medical or life sciences. Other scientific degree may be acceptable if associated with appropriate pharmaceutical industry experience. - Previous experience in the pharmaceutical industry or related to the conduct of clinical trials. - Solid understanding of the clinical drug development life cycle, including clinical trial design, operations and results analysis. - Demonstrated experience of clinical trial disclosure and transparency processes and systems, including a detailed understanding of the variable global requirements and the evolving landscape. - Sound ability to understand, interpret, critically analyze, and summarize complex scientific and medical data. This is an excellent opportunity to join a rapidly expanding pharmaceutical company. Please could you send any correspondence in English. Please quote reference 45353 in all correspondence.

Medical Device Development Project Leader - Basel Jasmin Baumgartner is recruiting for a Medical Device Development Project Leader join a global medical device company at their site based in Basel on a contract basis for 12 months with likelihood of extension. The main purpose of the role will be to: - Offer primary packaging and device expertise in a wider cross-functional drug product development team. - Lead Risk management activities. - Ensure a high-quality Design History file including the transfer of the Design History file to production. Further responsibilities will include: - Leading the definition of product requirements for packaging, medical devices, delivery systems, such as combination products in which the device is generally already registered but every so often needs to be developed. - Leading the collaboration with external development partners, such as monitoring of work progress according to plan. - Monitoring, supporting and challenge technical development as well as test and verification work. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - Bachelor's or Master degree in Packaging Science/Engineering or Mechanical Engineering or University level Engineering education. - Understanding of medical device regulations (FDA 21CFR 820, FDA 21CFR Part 4, EU Medical Device Directive, EU Medical Device Regulation). - Previous experience writing of technical documentation of drug/device combination products and medical devices, including Design Control process and other applicable regulatory, QA and GMP aspects. Please quote reference 45467 in all correspondence

John Crane ( - Teil der Smiths Group) ist ein weltweit führender Anbieter von Produkten und Dienstleistungen für die Prozessindustrie und die allgemeine Industrie. Seit der Gründung vor mehr als 95 Jahren hat sich das Unternehmen zu einem der bedeutendsten Lieferanten von Gleitringdichtungen, Versorgungssystemen, Hochleistungskupplungen und Stopfbuchspackungen entwickelt..... klicken sie bewerben, für die volle Stellenbeschreibung

Der Firmengründer unserer Mandantin lebte die Passion für Schweizer Qualität und Tradition. Seine Vision war es, das Sortiment in seinen Verkaufsgeschäften zu fairen Preisen, exzellentem Service und kompetenter Bedienung zu bieten. Heute, als Tochter einer führenden Firmengruppe in der Luxusgüterindustrie, führt unsere Mandantin in ihrer Ladenkette gut etablierte sowie moderne..... klicken sie bewerben, für die volle Stellenbeschreibung

Celonic AG is an internationally operating, rapidly growing service provider for the biotech industry. As a Contract Development and Manufacturing Organization (CDMO) we provide a broad portfolio of services to our global customers, ranging from Cell Line Development all the way up to GMP Manufacturing. We are empathic , efficient , and excellent . To us, this means that: We attentively listen to each other, our customers and our business partners, in order to obtain the best understanding of their exact needs or problems. We are transparent and flexible in our communication and our working processes, with a focus to always find the resource optimized way to the best solution. We always strive to be the best by far in every competitive environment. This philosophy applies to our products, our services, our behavior towards our customers and partners. For support of our USP Team at our Basel site (Switzerland) we are looking for Director (f/m/d) Upstream Processing (USP) Process Development Job description: Leading the complete USP Team responsible for Process Development Prove leadership for developing next-generation USP bio-solutions portfolio and platforms, including high throughput process development Actively support the yearly budgeting process for growth investments Providing in-depth upstream processing expertise to the team and actively engaging in trouble shooting activities Organizing asset and personnel resources Representing the USP Team in client meetings Supporting Sales and Project Management in realizing new customer projects Working on internal projects for continuously improving USP development strategy Reporting to the Vice President Biopharmaceutical Development Qualification and skills: Master or PhD in Biotechnology, Biochemistry or Biology Minimum 10 years experience with cultivation of mammalian cells Minimum 7 years industry experience in USP process development of biopharmaceuticals, GMP production experience favorable Proven capabilities in leading employees Experience with single-use bioreactors from mL-scale to 2000 L production scale, experience with automated multi-parallel bioreactors favorable Experiences in performance of process characterization and process validation favorable Vast experience with mammalian cell cultures (e.g. CHO, HEK and human cell lines) and thorough knowledge of cultivation techniques Empathic and solution oriented personality with sound communication skills and proven leadership experience Proven capabilities in working in interdisciplinary teams Excellent English skills, German skills favorable Our offer: Permanent employment Flexible working hours Corporate Fitness program Personal development based on individual capabilities Broad insight in various areas of development and manufacturing Corporate culture build on recognition, respect and empathy