43 English-speaking jobs in Hillerød

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.

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.

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.

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.

Postdoctoral Bioinformatician role bridging functional genomics and clinical population genetics. Lead CRISPR screen analysis and large-scale human genetic studies on biobank data. Requires PhD and expertise in high-throughput sequencing and genetic epidemiology.

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.

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.

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.

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.

Project Manager to lead analytical method transfer activities in a GMP Quality Control environment. This role coordinates cross-functional teams to ensure method transfers meet quality and compliance standards. Requires a relevant degree and experience in pharma/biotech method transfer.

Lead R&D team developing core optical and spectroscopic technologies, including NIR, LIBS, and computer vision. Requires technical background in optics/spectroscopy/vision, strong people management, and product development experience.

Senior Product Development Engineer develops primary packaging systems for parenteral products. This role translates regulatory and quality requirements into engineering solutions, managing technical documentation and stakeholder collaboration. Candidates need relevant experience in primary packaging development.

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.

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.

Lead end-to-end drug substance tech transfer into large-scale manufacturing. Drive compliant introduction of clinical, PPQ, and commercial processes, partnering with internal teams and customers. Requires 8+ years in CMC process development/GMP.

Lead a senior team to set direction and ensure flawless execution of technology transfer projects into large-scale manufacturing. Own strategy, planning, and execution while standardizing best practices.