37 English-speaking jobs in Hillerød

Lead Automation Engineer specializing in the AVEVA PI System within a GMP-regulated pharmaceutical environment. Responsibilities include technical leadership, architecture, configuration, and operational support for the PI system. Requires 5+ years of PI Historian implementation experience.

Leads scientific direction of internal and external communications for the pipeline. Oversees scientific content creation, ensures compliance, and builds relationships with KOLs and industry bodies. Manages a team of scientific affairs professionals. Requires an advanced degree in life sciences and 10+ years of experience in scientific/medical affairs.

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

Collect images of streets, points of interest, and public areas in EU countries using a vehicle equipped with 360 cameras. The project requires a valid driver's license, good driving skills, and the ability to follow specific routes.

Support computerised laboratory systems by aiding compliance, improving processes, and maintaining internal digital solutions. This role offers hands-on experience at the intersection of IT, laboratory operations, and compliance.

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.

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.

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

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.

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.

Experienced Risk Coordinator needed to support a major pharmaceutical commissioning, qualification, and startup project. Responsibilities include facilitating risk assessments, reviewing safety documentation, and ensuring safe execution of activities. Requires PSM background and pharma project experience.

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.

Seeking a Warehouse Assistant for a temporary, full-time role 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.

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.

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.

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.