27 English-speaking jobs in Hillerød

Develop innovative cloud-based services using C# and Microsoft Azure for FOSS IQX. Tasks include designing solutions, integrating third-party systems, and maintaining infrastructure using Infrastructure as Code.

Senior QA professional needed to be the primary customer contact for quality topics in Drug Substance, Drug Product, and Finished Goods manufacturing. Requires 10+ years of relevant QA experience and a Master's degree.

Global Support Specialist for advanced FTIR and Flow Cytometry instruments. Troubleshoot technical issues, create service documentation, and develop training for global service teams. Requires a technical background and strong communication skills.

Junior Project Manager to support and coordinate R&D projects across products and technologies. Responsibilities include managing development projects, prioritizing backlogs, and tracking milestones. Experience in a technical environment is preferred.

Associate Programme Director drives early delivery solution strategies for new drug assets, representing the final product perspective in Global Project Teams. This strategic role shapes development and commercial positioning.

Seeking a Software Engineer, Data Scientist, or Bioinformatician to support personalized medicine research. Responsibilities include data stewardship, research platform development, and data analysis for genomic and transcriptomic data.

Senior Risk Consultant to coordinate daily Risk Assessments and Method Statements for a large-scale Pharmaceutical CQV project. Requires PSM background, GMP familiarity, and experience with EHS in commissioning phases.

Drive early delivery solution strategies for 10-15 new drug assets. Represent the final product perspective in Global Project Teams, shaping development and commercial positioning. Requires a Master's degree and experience in complex program management.

Drive design control and risk management across the full medical device development lifecycle. Execute design control, manage requirements traceability, and ensure regulatory compliance with 21 CFR 820.30 and ISO 13485.

Nighttime Operators join biopharmaceutical production teams in Downstream and Upstream. Tasks include executing cGMP documents, batch documentation, and equipment preparation. Candidates should be detail-oriented and comfortable with GMP.

Lead a senior team to ensure flawless execution of technology transfer projects into large-scale manufacturing. Own strategy, planning, and execution while standardizing best practices and strengthening governance.

Data Visualization & Analysis Intern to transform manufacturing data into insights. Responsibilities include developing Power BI dashboards, supporting data analysis, and troubleshooting data pipelines. Requires studies in a quantitative field and Power BI experience.

Join the night shift as a Manufacturing Associate in Downstream and Upstream biopharmaceutical production. Tasks include executing cGMP documents, batch documentation, and equipment preparation. Requires attention to detail and ability to read English work instructions.

Consultancy in Cardiology combined with a 5-year clinical professorship focusing on Intensive Care in critical Heart Disease. Requires board-certified specialist in Internal Medicine: Cardiology.

Build and maintain BI solutions using Power BI, DAX, and SQL. Develop data solutions with SQL, Microsoft Fabric, and ADF, owning the data value chain from source systems to reporting.

Senior Technical Filling Professional takes ownership of production equipment, leading complex root cause investigations and driving continuous improvement in a GMP manufacturing environment. Requires engineering degree and experience with automated equipment.

Senior Systems Engineer needed for early-stage development projects. Requires a mechanical engineering background with experience in pen injectors or drug delivery systems. Responsibilities include requirements definition, risk analysis, and supporting design.

Senior Technical Filling Professional takes technical ownership of production equipment, leading complex root cause investigations and driving continuous improvement in a GMP manufacturing environment. Requires engineering degree and experience with automated equipment.

Lead a senior team to ensure flawless execution of technology transfer projects into large-scale manufacturing. Own strategy, planning, and execution while standardizing best practices and strengthening governance.

Three-year Postdoctoral Position in CRISPR-Based Genome Editing. Develop patient-tailored CRISPR therapy for Glanzmann thrombasthenia, spanning genetic characterization to preclinical model assessment. Requires PhD and strong CRISPR/cell biology experience.