118 English-speaking jobs in Hørsholm

Senior iOS Developer to join a team building a new golf app from the ground up. Experience with Swift, SwiftUI, and Agile development is required. Must have 5+ years of experience building and maintaining apps at scale. Kotlin Multi-platform experience is a plus.

Software Engineer to build and maintain CI/CD pipelines, tools, and platforms for developers. Requires strong Python and C++ skills, experience with build systems (CMake, Conan, Pip), and CI/CD tooling.

Develop virtual golf course environments in Unity, integrating vegetation and natural elements for realistic 3D experiences. Requires 2+ years of professional experience in Unity or Unreal game development and a portfolio demonstrating strong visual design skills in natural environments.

Lead a team of iOS developers in building the flagship Trackman Golf app for iOS and Android. Collaborate with product owners and UI/UX designers to craft intuitive, high-performance features. Deliver end-to-end functionality in a Kotlin Multiplatform codebase. Mentor developers, coordinate with other teams, and shape processes as the organization scales.

Design, build, and maintain efficient software in C++ and Python. Contribute to system-wide improvements and ensure reproducible builds.

Senior Patent Attorney to build and manage patent portfolios for a growing biopharmaceutical company. Responsibilities include patent landscape analysis, drafting and prosecuting patents, assessing FTO risks, and providing expert opinions to stakeholders. Requires a PhD in a relevant scientific field, EQE qualification, and at least eight years of experience in pharmaceutical patenting.

As a Procurement Data & Reporting Manager, you will design and implement data governance standards, develop insightful dashboards, and build reporting frameworks to empower global procurement decisions. You will collaborate with IT and stakeholders to ensure data accuracy and transparency.

Senior Director, Qualified Person, QA will lead a team of 40 employees and be responsible for QA oversight at Site Hørsholm. This role requires a minimum of 10 years of experience in quality, manufacturing, product development, or regulatory affairs within the pharmaceutical industry. The successful candidate will ensure regulatory and GMP compliance, contribute to business strategies related to quality, and develop and optimize quality processes.

Senior Global Medical Affairs Manager will develop and execute medical communication strategies for respiratory SLIT-tablet portfolio. Responsibilities include publication strategy, congress planning, KOL engagement, and supporting promotional materials development.

Lead and scale a remote sales team for a B2B SaaS platform focused on e-commerce marketing performance. Execute go-to-market strategy, drive sales performance, and shape sales culture. Proven experience leading B2B SaaS sales teams in a fast-growing scale-up is required.

Lead a team of rewards specialists and advise Executive Management on global compensation, benefits, and mobility strategies. Ensure alignment with employer brand and talent strategy, drive policy implementation, and maintain compliance with regulations.

Santen seeks a driven Country Manager for Norway & Denmark to lead commercial operations, including P&L ownership, sales leadership, and business performance. This hands-on role requires experience in pharmaceutical sales leadership, P&L responsibility, and a strong understanding of the Norwegian healthcare system.

Commercial Enablement IT Apprentice will coordinate website implementation, develop Power BI visuals, and automate business routines. The program provides practical experience with commercial features across EMEA and mentorship from an experienced IT Application Manager.

Develop sediment transport formulations for vegetated marine habitats (saltmarshes and eelgrass meadows) within the MIKE Powered by DHI modeling suite. Validate and/or verify formulations against existing data and disseminate results.

Senior Director of Scientific Model Development will lead the scientific direction and execution of non-GLP preclinical model development for a growing CRO. This role bridges science and business, ensuring alignment with market needs, technological opportunities, and operational capabilities. Responsibilities include leading model development, evaluating new technologies, identifying new disease areas, and representing the CRO externally.

Senior Scientific Project Manager to lead drug discovery projects from hit identification to development candidate selection. Responsibilities include critically assessing biological data, identifying project risks, and communicating project updates. Requires a PhD in life sciences and 5+ years of industry experience as a Project Manager leading drug discovery projects.

Lead DMPK specialist needed for peptide projects spanning in vitro, ex vivo, and in vivo experiments. Define and execute DMPK strategies from early discovery to First-in-Human studies. Shape and develop DMPK workflows and processes within a collaborative team environment.

Coordinates all shipments of biological samples and chemical materials, ensuring compliance with SOPs and regulations. Executes end-to-end shipment processes, prepares documentation, and manages shipment tracking. Supports incoming package registration, distribution, and procurement across departments.

Clinical Trial Coordinator to support expanding drug development activities. Responsibilities include maintaining trial documentation, coordinating logistics, and ensuring GCP compliance. Requires a bachelor's degree in a life science field and 2-3 years of clinical research experience. Experience with CROs, eTMF, and EDC systems is required.

Coordinate activities related to scientific studies, ensuring compound and formulation aspects are clarified before in vivo study start. Drive alignment, gather information, and contribute to compound calculation workflows. Present Gubra's formulation testing when relevant.