6848 English-speaking jobs in Capital Region of Denmark

Keyrock seeks a Head of Data to lead the strategic direction and operational excellence of the firm's trading data ecosystem. This role will ensure the quality, reliability, and scalability of data for trading, research, risk management, and decision-making.

Rust or C++ Engineer needed for low latency options trading system. 5+ years experience with scalable systems architecture and either Rust or C/C++. Options trading knowledge required.

The Tech Lead is a hybrid role combining hands-on engineering, architectural leadership, and team enablement. This role ensures delivery excellence by contributing to the codebase, guiding the team technically, and aligning execution with long-term strategic goals. The Tech Lead is accountable for technical execution and delivery quality, ensuring systems are built to high standards of reliability, performance, and maintainability.

Designs, implements, and maintains IT infrastructure solutions ensuring scalability, security, and efficiency.

Investor Relations Officer will translate complex financial and strategic information for the investment community. Collaborate with cross-functional teams to draft reports, prepare earnings calls, and investor presentations. Maintain key IR resources and actively participate in investor events and analyst briefings.

People Manager to oversee daily operations of Formulation Development department. Manage a team of scientists and technicians, ensuring smooth workflows, high-quality output, and regulatory compliance.

Senior/Principal Technician needed for API Development. Drive chemical process development from lab to pilot scale, support technology transfer projects, and perform synthesis, purification, and characterization of APIs. Must have laboratory technician education and experience in pharmaceutical or chemical development with solid understanding of CMC principles and GMP requirements.

The Global Regulatory Program Lead will design and implement comprehensive regulatory programs for rare disease treatments from early development through lifecycle management. Responsibilities include defining global regulatory pathways, leading Health Authority engagement, planning submissions, and mitigating regulatory risks.

This 2-year Graduate Programme offers four rotations in Finance, Marketing, and Supply Chain. You will gain hands-on experience, work with global teams, and develop a deep understanding of LEO Pharma and the pharmaceutical industry. The programme includes mentoring, a development plan, and opportunities for international assignments.

Lead global rewards strategy, design, and governance for LEO Pharma's total rewards function. Oversee job architecture, executive compensation, mobility programs, and regulatory compliance.

As an HR Business Partner, you will act as a trusted advisor to senior leaders, driving HR initiatives and providing data-driven insights to enhance business value. You will collaborate with global HR teams and leverage your expertise in Danish employment law and labor relations.

Lead biostatistical strategy and execution across clinical development projects. Provide input to programs, design trials, mentor colleagues, and influence global asset strategy.

AI & Data Scientist will design and implement AI solutions across various business areas. Responsibilities include developing models, collaborating with teams, and leveraging expertise in Python, ML, and cloud technologies.

Ensures compliance with GCP regulations and maintains quality standards. Approves QMS documentation and acts as a host during inspections. Provides GCP guidance and training to stakeholders.

Senior Project Manager will lead strategic projects critical to LEO Pharma's ability to deliver high-quality products. Responsibilities include leading cross-functional project teams, driving project scope alignment, and managing technology transfers and new product introductions.

The Senior Principal Regulatory Devices Lead will define global regulatory strategies for Drug Device Combination Products in development and during life-cycle maintenance. Responsibilities include leading cross-functional alignment, ensuring compliance with FDA, EMA, EU MDR, and other applicable global standards, and engaging with regulatory authorities.

Lead and develop a global HRBP function for assigned business areas, shaping people strategy and driving business outcomes.

Leads global medical strategy framework development and execution across therapeutic areas, ensuring alignment with business goals and driving medical excellence.

Leads and executes investigations into ADME properties for early and late-stage drug development projects. Provides holistic DMPK support to development teams across absorption studies, metabolism profiling, and drug-drug interaction understanding. Designs and executes studies to optimize ADME properties in topical and systemic drug products. Applies and interprets PK/PD modeling tools to inform exposure-effect relationships. Coordinates and manages studies with external CROs. Shapes skin PK strategies for profiling compounds.

Student Assistant to support the Commercial Strategy team. Responsibilities include managing market data, collaborating with global teams, and preparing reports. Requires strong organizational skills, attention to detail, and proficiency in Microsoft Office Suite. Must be a currently enrolled student with at least 2 years remaining in studies.