41 English-speaking jobs in Hillerød

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 experience with design control principles and medical device regulations.

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

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 the Drug Substance Manufacturing team in Downstream and Upstream Production. Responsibilities include executing cGMP documents, batch documentation, and process equipment preparation. Candidates should be focused and understand process flows.

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

Drive end-to-end tech transfer for new drug substance programs into large-scale manufacturing. Lead cross-functional efforts, manage project plans, and ensure compliance with GMP requirements. Requires 8+ years in CMC process development.

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 operational sources to reporting.

Full-time 3-year position assisting AI researchers with image analysis and data processing at DEPICT. Requires strong programming skills, Linux experience, and prior Deep Learning model development experience.

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

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 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.

Implement and operate the ISO 27001:2022-certified ISMS, driving control implementation across business units. Validate controls, support audits, and maintain documentation. Requires knowledge of ISO 27001/27002 and professional English.

Automation Engineer needed to program, develop, and validate automation systems, specializing in Emerson DeltaV. Responsibilities include system design, troubleshooting, and providing technical support within the pharmaceutical industry. A relevant engineering degree is required.

Lead a senior team to ensure flawless execution of technology transfer projects into large-scale manufacturing. Own strategy, governance, and cross-functional alignment for new program introductions.