36 English-speaking jobs in Hillerød

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.

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.

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.

Senior QA professional needed to be the primary quality contact for biopharma customers during commercial and Tech Transfer programs. Drive discussions on deviations, CAPAs, and complaints. Requires 10+ years of relevant QA experience.

Technical Specialist for Diagnostic Systems, R&D. Support testing, documentation, and maintenance for the ImmuView® Reader and diagnostic assays. Contribute to new assay development and equipment testing.

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.

Lead R&D for NIR, LIBS, and Vision technology teams, managing scientists and engineers. Develop core optical and spectroscopic technologies while aligning the technology pipeline with R&D strategy.

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.

This role combines a Neurology consultancy at Copenhagen University Hospital with a 10-year Clinical Professorship at the University of Copenhagen. Applicants must be board-certified specialists in Neurology and secure both appointments.

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.

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.

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.

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.

Senior QA Associate provides quality oversight for Materials, Supply Chain, and Warehouse operations, focusing on material qualification and new material onboarding for GMP manufacturing. Requires 7+ years in pharma/biotech with strong GMP knowledge.

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.

This role coordinates technical improvement activities in a regulated manufacturing environment. You will support investigations, maintain GMP documentation, and drive continuous improvement initiatives. A relevant degree and manufacturing experience are ideal.

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.