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- ...Switzerland. Novartis is unable to offer relocation support: please only apply if accessible. Are you ready to shape the future of regulatory precision medicine? As a Regulatory Diagnostics Senior Manager at Novartis, you’ll play a pivotal role in advancing our...Consigliato
- ...brighter future to look forward to. Apply today and join us in reimagining new medicines together! The Role: As Global Program Regulatory Director, you will provide global leadership throughout the lifecycle of a development and/or marketed product program(s). Your...ConsigliatoAssicurazione per l'invalidità
- Founded in 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 ...ConsigliatoApprendistato
- ...Molecule production, including internal and supplier specifications, regulatory filings, and collaboration with QC and technical experts... ...Opportunity: The Direct Material Data & Risk Analytics Specialist supports PT-wide risk management through hands-on material assessments...ConsigliatoLavoro a turni
- Summary Werden Sie Teil unseres Teams als Documentation Specialist GMP Sie haben ein Auge fürs Detail, arbeiten gerne strukturiert und möchten aktiv zur Qualitätssicherung in einem GMP-regulierten Umfeld beitragen? Dann sind Sie bei uns genau richtig! Als...Consigliato
- At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally ...Consigliato
- ...HPLC, Capillary Electrophoresis, UV) ensuring compliance with regulatory requirements Maintain excellent planning and collaboration... ...project team members (e.g. laboratory analysts, production specialists, manufacturing science and technology, quality assurance, regulatory...Consigliato
- ...Client: Our client, a successful and internationally operating Swiss company in FMCG in the Basel area, is looking for a Master Data Specialist (d/f/m) to join their global team, in a temporary assignment with start asap (ideally May/June) for the next 6 months. In this...ConsigliatoTemporaneoLavoro urgente
- ...for master data maintenance and transaction processing on the global treasury SAP system. We are hiring for two InHouse Bank Specialist positions on a temporary basis. The contract duration will be 12 months with the option of being extended. This role focuses...ConsigliatoTemporaneoOrario flessibile
- ...sense of urgency as a part of a matrix team, collaborating with specialists from each of our therapeutic disease areas and functions to... ...and advanced QC processes while ensuring adherence to SOPs, regulatory guidelines, and ethical standards for stem cell and organoid...Consigliato
- ...solutions to resolve issues for our partners (e.g., Quality, Regulatory, Manufacturing). Junior Technical Lead: As a Junior Technical... ...with data scientists, data engineers, UX/UI designers, IT specialists, and SMEs. Aid in value tracking and capability building....Consigliato
- ...drug development and ability to deliver impactful evidence for regulatory, market access, and clinical adoption. Experience with... ...opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page....Consigliato
- ...ensure seamless integration while maintaining compliance with regulatory standards. Please note that to be considered for this... ...opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. Hobson Prior is a leading...Consigliato
- ...business outcomes. Lead an organisation consisting of 170+ specialists and scientific staff based in South San Francisco (US) and in... ...PT (Commercial Manufacturing, CGT, Quality, Supply Chain. Regulatory) to ensure seamless product development, process and knowledge...Consigliato
- ...pharmaceutical facilities and maintenance environment. Knowledge and understanding of Good Laboratory Practices (GLP) and other regulatory regulations regarding facility operations. Business - High level of facility/utility operations and the ability to understand...ConsigliatoTemporaneo
- ...multiple indications, spanning multiple products. Lead multidisciplinary team of functional experts focused on securing global regulatory approval, market access and optimized commercial value of the program, while ensuring quality, compliance (internal and external)...Temporaneo
- ...in the assigned project or section of a clinical program Leading development of clinical sections of trial and program level regulatory documents Driving execution of the assigned clinical program and/or clinical trial in partnership with global line functions,...Assicurazione per l'invalidità
- .... If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching...
- ...evaluation of facts, adherence to investigative protocols, and timely resolution of issues in alignment with company policies and regulatory requirements. Provide expert legal advice on cross-border disputes, international investigations and related legal issues,...
- ...connecting microscopy users across campus and helping to build a vibrant, engaged user community. Collaborate with image analysis specialists to assist researchers in the initial stages of image processing and data analysis Further capabilities: Practice efficient...Lavoro post-doc
- ...International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use )ICH) / Good Clinical Practice (GCP) and regulatory requirements. The role may support larger scope projects and governance in SSU as applicable About the Role...
- ...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 program level regulatory...CDD
- ...If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page. Proclinical is a leading life sciences recruiter focused on finding exceptional...Apprendistato
- ...Authorities. The opportunity: In this role you will have considerable cross-functional interaction, notably including QA, Regulatory Affairs, Clinical and Commercial functions. This role reports to the Section Head of Device Engineering and is integrated into...
- ...allocation and capacity. Deep experience in pharmaceutical development from early to late phase incl. handover to production. Knows regulatory requirements and future trends; ensures full compliance of the operation. Setup a structure and mindset of continuous...
- ...from the date of receiving their PhD (i.e. PhD degrees must have been awarded June 2023 or later). Experience in understanding regulatory complexes using protein-based approaches as well as functional cellular assays. Strong publication record or other scientific...Lavoro post-doc
- ...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 dossiers,...Assicurazione per l'invalidità
- ...and trusted relationships with Pharmaceutical Development, External Manufacturing, Marketing, Supply Chain, Packaging Operations, Regulatory, etc. The Group Leader will lead a diverse group of individual contributors in packaging development. In addition to...
- ...functional communications to align with global strategy and leads the development of clinical sections of trial and program level regulatory documents • Acts as the medical expert, engages interactions with external stakeholders (e.g., regulatory authorities, key...
- ...programs Act as CEO of the company’s captive reinsurance company, Syngenta Rückversicherung AG, ensuring optimal risk retention and regulatory compliance Accountabilities: Global Insurance Risk Management Ensure comprehensive and consistent insurance or financial...Tempo pieno