45 English-speaking jobs in Hillerød

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

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

Consultancy in Neurology combined with a 10-year Clinical Professorship at the University of Copenhagen. The role requires a board-certified specialist in Neurology to contribute to clinical research, teaching, and departmental development.

Senior Risk Coordinator for a Pharmaceutical CQV project. Manage daily RAMS, conduct risk assessments, and review method statements on-site. Requires PSM background and experience in GMP environments.

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.

Senior IT Security Advisor leads cybersecurity strategy across six API manufacturing sites. This role ensures robust protection of IT and OT systems while maintaining regulatory compliance in a highly regulated environment.

Motivated night shift Operators join Downstream and Upstream biopharmaceutical production. Tasks include executing cGMP documents, batch documentation, and equipment preparation. Requires attention to detail and ability to follow English work instructions.

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.

Drive design control and risk management across the full product development lifecycle for medical devices. Execute design control, manage requirements traceability, and ensure regulatory compliance.

Lead a senior team to set direction and ensure flawless execution of technology transfer projects into large-scale manufacturing. Own strategy, governance, and best practices for TT. Requires 12+ years in pharma/biotech CMC and 7+ years in people leadership.

Drive design control and risk management across the full product development lifecycle for medical devices. Execute design control, maintain requirements traceability, and ensure regulatory compliance. Requires experience in medical device development.

Experienced Risk Coordinator needed for a 6-month pharmaceutical project. This role focuses on risk assessment, process safety, and control of work during commissioning and qualification. Requires 5+ years in EHS or pharmaceutical project experience.

Data Visualization & Analysis Intern role supporting data-driven decision-making using manufacturing data. Responsibilities include developing Power BI dashboards and supporting data analysis. Requires studies in a quantitative field and Power BI experience.

Senior IT Security Advisor leads cybersecurity strategy and risk management across six API manufacturing sites. This role advises stakeholders on IT and OT security, ensuring compliance with GMP/GxP and embedding security-by-design.

Coordinate technical improvement activities and support deviation investigations in a regulated manufacturing environment. This role requires strong organizational skills, technical understanding, and stakeholder collaboration.

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.

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

Consultant in Cardiology combined with a 5-year Clinical Professorship in Intensive Care in Critical Heart Disease. Requires board-certified specialist in Internal Medicine: Cardiology.