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Les résultats de la recherche: 32 offres d'emploi
- ...tätiges Life Science Unternehmen mit Spezialisierung auf Pharma/Biotech, suchen wir ab sofort eine/n Experte/in im Bereich «Automation Engineering». Job Description: Sie werden direkt an den Head of Electrical Engineering berichten und haben als Automation Engineer eine...SuggéréTemporaireRecrutement immédiat
- ...Switzerland in 1968, Zühlke is owned by its partners and located across Europe and Asia. We are a global transformation partner, with engineering and innovation in our DNA. We're trusted to help clients envision and build their businesses for the future – to run smarter...Suggéré
- ...and Drug Delivery Systems. The (Senior) Principal Process Engineer and Strategy Realization Lead ensures robust clinical and... ...Technical Operations network partners is crucial for success. A key component of the role involves providing strategic guidance across the...Suggéré
- ....NET Software Engineer - Software House - Basel, Switzerland (Tech stack: .NET Software Engineer, .NET 9, C#, Blazor, Azure, JavaScript, HTML5, CSS3, Agile, Programmer, Full Stack Developer, Architect, Softwareentwickler, Entwickler, .NET Software Engineer) Do you want...SuggéréTemps pleinRemote jobPoste du soir
- ...is responsible for the development and support of drug delivery devices for the product portfolio. Our activities span a range of engineering disciplines from the requirements definition phase through to commercialization and marketed product support. The Device...Suggéré
- ...this challenge by enhancing maturation and introducing aging components is critical for creating more accurate and effective models... ...: • PhD in molecular biology, neuroscience, tissue engineering, or a related field • Note that PhD students in the last year...SuggéréEmploi postdocEn septembre
- ...to come. Join Roche, where every voice matters. The Position The Analytical Research & Development department, an integral component of Synthetic Molecules Technical Development, bears global responsibility for the advancement of cutting-edge analytical...Suggéré
- ...or sub studies consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications • Leading development of clinical sections of trial and...SuggéréCDD
- ...Deliverables may include sections of individual protocols consistent with the IDP, data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., IBs, Brochures, briefing books, safety updates,...SuggéréAssurance-invalidité
- ...monitoring Maintain REFM-related governance frameworks, policies, norms, and compliance standards Collaborate with procurement and engineering teams to ensure seamless service delivery Organise and lead regular service review meetings with external providers...SuggéréTemporaire
- ...in due-diligence teams to evaluate in-licensing opportunities Essential Requirements: Ph.D. in pharmacology, biology, engineering, mathematics, statistics, or a field with significant modeling-related content (or equivalent) with 6+ years’ experience in clinical...Suggéré
- ...Deliverables may include sections of individual protocols consistent with the IDP, data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., IBs, Brochures, briefing books, safety updates, submission...SuggéréAssurance-invalidité
- ...Switzerland in 1968, Zühlke is owned by its partners and located across Europe and Asia. We are a global transformation partner, with engineering and innovation in our DNA. We're trusted to help clients envision and build their businesses for the future – to run smarter...Suggéréà domicileTravail à domicileHoraire flexible
- ...ability to effectively work with health authorities. You understand and have experience with the majority of clinical pharmacology components, as well as some filing experience. You have solid experience in regulatory interactions with examples of health authority...Suggéré
- ...regulatory approval/market access for one or multiple treatment indications and/or multiple programs Leads the creation of clinical components of key documents (e.g., Clinical Trial Protocols (CTPs), Investigator’s Brochures, Clinical Study Reports (CSRs), regulatory...SuggéréRemote jobAssurance-invalidité
- ...Switzerland in 1968, Zühlke is owned by its partners and located across Europe and Asia. We are a global transformation partner, with engineering and innovation in our DNA. We're trusted to help clients envision and build their businesses for the future – to run smarter...Remote jobHoraire flexible
- ...Accelerate operational excellence in Value and Access (V&A) by streamlining global operations and reporting, developing a robust delivery engine, and a worldclass Learning experience of associates globally across 100+ countries. Leadership of BSI V&A organisation to ensure...
- ...Switzerland in 1968, Zühlke is owned by its partners and located across Europe and Asia. We are a global transformation partner, with engineering and innovation in our DNA. We're trusted to help clients envision and build their businesses for the future – to run smarter...Apprentissage
- ...through collaboration with our scientists and partners. Thrive in an interdisciplinary environment, working alongside biologists, engineers, and other computational scientists. The position is fully funded for 5 years, supporting a group size of 4 members plus 1 PI...Emploi postdocEn aoûtEn septembre
- ...Discovery”): Develop, in collaboration with TM TA Head and work with teams to carry out, strategies for the Translational Medicine component of drug development projects from Research to TDP in single or multiple indications, including post-indication expansion projects....
