790 English-speaking jobs in Basel

Large Molecule Bioanalytical Manager page is loadedLarge Molecule Bioanalytical Manager Apply locations Welwyn time type Full time posted on Posted 2 Days Ago time left to apply End Date: July 18, 2025 (19 days left to apply) job requisition id 202506-115171At 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 and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

Executive Director, Oncology Cell & Gene Therapies 2 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features.

About Straumann Group Straumann collaborate with passionate people who fit in with the agile dynamics of our size-for-success company. People at Straumann appreciate the opportunity to shape our future and create impact. Encouraging leadership and inspiring ideas from our people has guided us through our proud history of pioneering innovations.

Job Description Summary Location: Basel, Switzerland Role Purpose: As Senior Expert / Functional Lead (FL) you will play a key role in the development of formulations and processes for Biologic Drug Products (e. g. therapeutic proteins, conjugates and other new modalities) for clinical or commercial use.

Job Description Summary This key director for strategy role will enable and drive the creation of the data & digital strategy for Biomedical Research in alignment with the Novartis AI strategy and will ensure execution of it by designing the required strategic initiatives driven by the Data & Digital Office.

Our client based in Basel (Switzerland) is looking for an Animal Keeper to look after and caring for laboratory animals. This position includes Shift work on weekends and public holidays (365 day operation). Responsibilities: • Independently responsible for cleaning and disinfecting operating facilities and cage material.

At Mace, our purpose is to redefine the boundaries of ambition. We believe in creating places that are responsible, bringing transformative impact to our people, communities and societies across the globe. To learn more about our purpose, culture, and priorities, visit our strategy site.

Position status:This opportunity is for a bid, so it is not yet a secured role. If you would like to be considered as we progress with this position, please click to apply. At Mace, our purpose is to redefine the boundaries of ambition. We believe in creating places that are responsible, bringing transformative impact to our people, communities and societies across the globe.

ABOUT STRAUMANN GROUP Straumann collaborates with passionate people who thrive in the dynamic environment of our successful company. Our team values the opportunity to shape the future and make an impact. We foster leadership and inspire innovative ideas, guiding us through a proud history of pioneering advancements.

Position Overview We are seeking a visionary and strategic Head of Implant Treatment Workflow Management to lead the development, enhancement, and execution of our dental implant workflow solutions.

at the Friedrich Miescher Institute for Biomedical Research (FMI) is seeking a motivated Research Assistant specializing in genome engineering of mammalian cells to support current and future projects in the lab. The Giorgetti group studies how the three-dimensional folding of mammalian genomes controls gene expression — specifically, how enhancer sequences control transcription from promoters.

Job Description At Agilent, we’re on a collective quest to improve the world around us. As a global leader in laboratory technologies, we support scientists in 110 countries in cutting-edge life science research, patient diagnostics and their efforts to ensure the safety of water, food and pharmaceuticals.

Contract duration: 1 year Responsibilities: Overseeing the creation, maintenance, and quality of the Trial Master File, a collection of essential documents for a clinical trial and TMF archival Ensuring TMF documents are accurate, complete, and compliant with regulations (e. g. , ICH/GCP) and internal/external SOPs.

Direct message the job poster from Coopers Group AG Talent Acquisition Consultant at Coopers Group AG - Life Science Contract duration: 1 year Travel: Ready to travel internationally - Europe, US, APAC- 10-20% The CTSM provides oversight and/or manages the supply chain of Investigational products from finished Drug product including ancillary devices to returned or destroyed IP kits.

10+ years in field-based, customer-facing roles with increasing responsibility. Proven success in global strategic/key account management at executive level. Excellent communicator with strong strategic thinking and project management skills. Ability to lead across a matrixed organization and influence stakeholders. Global mindset with sensitivity to cultural and organizational complexity.

Viking was founded in 1997 and provides destination-focused voyages on oceans, rivers and lakes around the world. Designed for experienced travelers with interests in science, history, culture and cuisine, Chairman Torstein Hagen often says Viking offers experiences for The Thinking Person®.

Job Description Summary The Clinical Development Medical Director (CDMD) is the clinical leader of a section of a clinical program (e. g. , an indication, a new formulation, or a specific development phase), or a large, complex trial, under the leadership of the (Sr. ) GPCH.

Director Data & Digital Strategy (Biomedical Research) Job ID REQ-10054625 Summary This key director for strategy role will enable and drive the creation of the data & digital strategy for Biomedical Research in alignment with the Novartis AI strategy and will ensure execution of it by designing the required strategic initiatives driven by the Data & Digital Office.

The Clinical Development Director (CDD) in the Cardio Renal & Metabolic (CRM) Development Unit is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As a CDD in the CV TA, you will oversee clinical development for the assigned programs and drive the execution of the clinical development plan.