39 English-speaking jobs in Hillerød

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.

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.

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.

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 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 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 leading systems engineering, requirements definition, and risk analysis.

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 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.

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.

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

Commissioning Manager responsible for planning and governing post-construction commissioning activities on complex projects. Requires strong understanding of RAMS, LOTO, and HSE to ensure safe execution and transition to operational readiness.

The CQV Permit Office Manager controls permit-to-work, LOTO, and safety governance during complex construction commissioning. This role ensures structured, compliant execution, acting as the interface between construction completion and operational readiness.

Three-year Postdoctoral Position in CRISPR-Based Genome Editing. Develop patient-tailored CRISPR therapy for Glanzmann thrombasthenia, focusing on translational workflow and preclinical assessment. Requires PhD and strong CRISPR/cell biology experience.

R&D Director for Grain & Feed oversees all NPD projects, managing the core team. This role requires leading cross-functional projects spanning engineering, software, and data science to bring innovative analytical solutions to market.

Experienced CQV Consultant needed to lead the development of a Master Validation Plan for a Drug Product programme. This hands-on contract role requires expertise in equipment and process validation within GMP environments.

Experienced CQV professional needed for a contract role supporting Drug Product validation. Responsibilities include developing re-validation strategies, technical oversight, and coordinating cross-functional stakeholders in a GMP manufacturing environment.