47 English-speaking jobs in Hillerød

Experienced Risk Specialist needed for large pharma project in Copenhagen. Oversee and perform health and safety and risk management activities. Ensure compliance with GMP, HSE legislation, and industry best practices. Support development and maintenance of Process Safety Management systems. Collaborate with cross-functional teams to integrate risk management processes.

Leads NPD projects for the Grain & Feed business unit, overseeing all aspects from concept development to market implementation. Manages a core team and collaborates with cross-functional stakeholders, including mechanical engineering, electronics, software development, and data science. Ensures projects meet customer needs, support business goals, and drive successful product launches.

Student Assistant will support the Downstream Process Engineering team with tasks such as documentation, data analysis, and process improvement projects. The role requires on-site presence and proficiency in Microsoft Office.

Lead a new Operation Support team providing 24/7 support to Drug Substance Manufacturing. Establish operating models for first-line support, ensuring operational stability and driving plan adherence. Resolve complex issues, coordinate cross-functional responses, and facilitate continuous improvement.

Manufacturing Expert to support daily production in a fast-paced 24/7 environment. Responsibilities include issue resolution, adherence to production plans, and data analysis to improve quality and efficiency.

Pre or Postdoctoral researcher to run and coordinate studies on eating disorder risk using longitudinal data. Develop study protocols, lead data analysis, and write manuscripts. Supervise junior colleagues and collaborate with partners. Requires PhD with experience in eating disorders, longitudinal data analysis, and psychiatric epidemiology.

Senior QA Associate to support Drug Product Manufacturing operations. Manage quality records, review deviations and CAPAs, and ensure compliance with GMP standards. Requires 5+ years of QA experience in pharmaceutical manufacturing.

Senior researcher position in physiotherapy at Copenhagen University Hospital – North Zealand combined with a part-time professorship at the University of Copenhagen. Applicants must be a board-certified registered physiotherapist with a PhD and experience in quantitative research methods, physical activity research, and chronic disease treatment.

Software Developer needed to design, develop, and maintain scalable, secure solutions. Experience with cloud platforms (Azure, AWS, GCP), DevOps tools (Terraform, Docker, GitHub), and programming languages (C#, Java, TypeScript) required.

Student Assistant to support commercial platforms, data, and processes. Will create user guides, maintain data quality, and lead a project focused on commercial processes. Requires strong Microsoft Office skills, excellent communication, and familiarity with enterprise systems.

Validation Engineer needed for temporary position (ending 31.03.2027). Prepare, execute, and finalize validation protocols for equipment and processes. Investigate deviations, drive CAPA, and ensure compliance with regulatory expectations. Lead cross-site validation improvements and mentor junior staff.

Lead a team of nine Investigators overseeing deviations for a single API production line (cell culture through purification). Optimize the deviation process, reduce lead time, and strengthen quality and audit readiness while maintaining GMP compliance.

Lead a team of 30+ Manufacturing Associates in Drug Substance Manufacturing. Provide shop-floor leadership, training, and development. Drive continuous improvement and problem-solving. Experience in pharmaceutical manufacturing and LEAN principles required.

Lead and develop teams of operators in Filling and Formulation within a Drug Product Manufacturing facility. Ensure cGMP compliance, quality, and a safe work environment. Manage team growth, competencies, and cross-collaboration.

Leads and manages the strategic vision for the bioreactor scale-up team. Develops and executes methodologies for scaling cell culture processes from bench-top to large-scale bioreactors. Serves as the primary point of contact for customers regarding process scaling.

Internship in Manufacturing Sciences and Technology – Drug Product supporting aseptic production equipment activities. Tasks include measuring plunger insertion, providing input to work instructions, and handling inspection samples.

Lead and develop a team of nine Investigators, managing workload and ensuring high-quality investigations and CAPAs across cell culture through purification. Drive standard work, visual management, and performance metrics. Optimize handovers and escalation paths with Manufacturing and QA. Promote cross-training and continuous improvement initiatives.

Validation Engineer needed for temporary position ending March 31, 2027. Prepares, executes, and finalizes validation protocols and reports for equipment and processes. Investigates deviations, conducts root-cause analysis, and drives CAPA implementation. Requires 3-5 years of validation/qualification experience, preferably including cleaning validation. Strong understanding of regulatory requirements and guidance. Excellent cross-functional collaboration and communication skills.

Leads risk-based validation activities for Drug Product and Finished Goods, including equipment, processes, utilities, and computerized systems. Prepares and executes validation protocols and documentation. Acts as a Validation Subject Matter Expert, defining strategies and ensuring compliance with global standards.

Leads a new Operation Support team providing 24/7 support to Drug Substance Manufacturing, ensuring safe, compliant, and efficient production. Drives issue resolution, removes obstacles, and ensures seamless production execution through collaboration with Production Leaders, Value Stream Directors, and cross-functional partners.