40 English-speaking jobs in Hillerød

Strategic leader to shape policy and drive results in Drug Product and Finished Goods. Manage engineers, improve equipment performance, and establish operational structures. Requires 6+ years of management experience.

Validation Engineer joins the Downstream team to ensure equipment readiness for production. Responsibilities include writing IQ/OQ/PQ protocols, managing change controls, and executing cleaning validation. Requires 3-5 years of industry experience.

Develop primary packaging systems for parenteral products, translating regulatory and quality requirements into engineering solutions. Prepare technical documentation and collaborate with stakeholders to ensure compliance and functionality.

Material Scientist role involving assessing new materials, virology assessments, and documenting results. Requires MSc/PhD in a related science and fluency in English.

Strategic leader to manage Drug Product and Finished Goods engineering. Establish operations, improve performance via problem-solving, and guide teams in a growing manufacturing environment.

Senior QA for QC Specialist requires 15+ years of experience providing deep quality oversight of QC activities. Responsibilities include reviewing complex documentation, driving risk-based decisions, and partnering with QC to strengthen compliance.

Experienced Risk Coordinator needed for a pharmaceutical project during turnover, commissioning, and CQV. Responsibilities include coordinating daily RAMS, conducting risk assessments, and ensuring safe execution of activities. Requires EHS background and familiarity with pharmaceutical regulations.

Serve as Global Support Specialist for advanced FTIR and Flow Cytometry instruments. Create documentation, develop training, and manage service protocols while linking development and field service teams.

Strategic leader to manage Drug Product and Finished Goods Engineers. Focus on improving equipment performance, establishing operational structures, and executing company policies in a growing manufacturing area.

Develop innovative cloud services for food analytics using C# and Azure. Design solutions, integrate third-party systems like SAP, and maintain infrastructure using Infrastructure as Code. Requires 5+ years in C#/.NET.

Validation Engineer needed for the Downstream team. Responsibilities include writing/reviewing IQ, OQ, PQ protocols, participating in PPQs, and executing cleaning validation. Requires a Bachelor's degree and 3-5 years of industry experience.

Strategic leader to shape policy and drive results in Drug Product, Finished Goods, and Tech Transfer Engineering. Focus on improving equipment performance and developing necessary structures. Requires 6+ years of management experience.

Seeking a Warehouse Assistant for a temporary, full-time position at a tire center. Duties include handling, sorting, and moving tires, plus general warehouse tasks. Must be physically fit, reliable, and speak Danish or English.

Validation Engineer needed for the Downstream team. Participate in PPQs, capex changes, and audits. Write/review IQ, OQ, PQ protocols and manage cleaning validation. Requires 3-5 years of industry experience.

Advanced Test Engineer to plan, execute, and document design verification for medical devices and primary packaging. Requires engineering degree and experience in testing within product development projects.

Experienced Risk Coordinator needed for a pharmaceutical project supporting turnover, commissioning, and CQV. Responsibilities include coordinating daily RAMS, conducting risk assessments, and ensuring safe execution of activities.

Advanced Product Development Engineer role focusing on medical device development and lifecycle management. Requires an engineering degree and experience in regulated environments. Responsibilities include technical issue investigation and cross-functional collaboration.

Own the full lifecycle of design verification and shelf-life testing for medical device and packaging projects. Lead testing, author protocols, and analyze data to ensure products meet requirements. Requires an Engineering degree and experience in testing.

Develop primary packaging systems for parenteral products, translating regulatory and quality requirements into engineering solutions. Prepare technical documentation and collaborate with stakeholders to ensure compliance and safety.

Experienced Risk Coordinator needed for a pharmaceutical project during turnover, commissioning, and CQV. Responsibilities include coordinating daily RAMS, facilitating risk assessments, and ensuring safe execution of activities.