41 English-speaking jobs in Hillerød

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.

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.

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.

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.

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.

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.

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.

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.

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 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.

Experienced Validation Engineer/SME needed for Controlled Temperature Units (CTUs) like refrigerators. Drive validation strategy, ensure regulatory compliance, and lead IQ/OQ/RQ activities within the life science industry.

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.