37 English-speaking jobs in Hillerød

You will also head up the responsibility of Engineers covering Assembly and Packaging. Main focuses are in Drug Product, where we need to learn our equipment and improve its performance by systematic problem solving and develop missing structure to support required development. If you want to lead high-impact operations across multiple functional areas, then take a closer look.

Join our QA for QC team at FUJIFILM Biotechnologies in Hillerød as a Senior QA for QC Specialist, supporting our QC laboratory in this newly created position. As our production site grows, QC expands, which requires increased quality oversight. We are looking for the right Senior QA for QC Specialist who would like to be part of a positive, engaged, and supportive team.

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.

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.

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.

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.

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.

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.

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 the Bioreactor Scale-Up team, setting global vision using expertise in cell culture process modeling and simulation. Drive projects from bench to production scale while serving as a primary customer contact.