36 English-speaking jobs in Hillerød

Drive early delivery solution strategies for 10-15 new drug assets in Drug Delivery Innovation. Represent the final product perspective in Global Project Teams, shaping strategic decisions across the pipeline.

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

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

Drive design control and risk management across the full product development lifecycle for medical devices. Execute design control, maintain traceability, and conduct verification/validation. Requires medical device development experience and knowledge of ISO 13485.

Lead a senior team to ensure flawless execution of technology transfer projects into large-scale manufacturing. Own strategy, governance, and best practices for TT, accelerating time-to-plant while maintaining quality and compliance.

Motivated Nighttime Operators needed for Downstream and Upstream biopharmaceutical production. Tasks include executing cGMP documents, batch documentation, and equipment preparation. Experience in pharma or Life Science background preferred.

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.

Experienced Risk Coordinator needed for a 6-month pharmaceutical project. Focus on risk assessment, process safety, and control of work during commissioning and qualification. Requires 5+ years in EHS within regulated environments.

Drive design control and risk management across the full product development lifecycle for medical devices. Key duties include executing design control, maintaining traceability, and conducting design reviews. Requires medical device development experience and knowledge of ISO 13485.

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.

This role coordinates technical improvement activities in a highly regulated manufacturing environment. Responsibilities include supporting deviation investigations, maintaining GMP documentation, and driving continuous improvement initiatives. A relevant degree and manufacturing experience are ideal.

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.

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.

Motivated night shift operators needed for Downstream and Upstream biopharmaceutical production. Duties include cGMP document execution, batch documentation, and process equipment preparation. Pharmaceutical or Life Science graduate preferred.

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.

A 3-year position as a Data Scientist at DEPICT focuses on assisting AI researchers with image analysis and data processing. Tasks include data handling, segmentation support, and managing AI training architecture.

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 background and troubleshooting skills.

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.

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 relevant engineering degree and experience with automated equipment.