44 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 to support Commercial Excellence team with systems enablement, reporting, and process improvements. Will own and deliver a project focused on commercial data, reporting, or automation. Requires data analysis, visualization, and strong communication skills.

Formulation Operator will execute formulation processes, support batch preparation and documentation, and contribute to operational improvements within a GMP-regulated environment.

Production Leader guides rotating day and night shifts, overseeing 24-30 Manufacturing Associates. The role requires a flexible leader who can work odd hours due to the 5/2 color-shift rotation. Responsibilities include team development, communication, problem solving, and ensuring safe production. Experience leading diverse teams in a production environment is required. High proficiency in English is essential.

Automation Engineer needed for a pharmaceutical project in Copenhagen. Design, configure, and implement automation systems, specializing in Emerson DeltaV. Troubleshoot, provide support, and collaborate with teams. Bachelor's degree in Automation Engineering, Electrical Engineering, or related field required. Experience with DeltaV and GMP is preferred.

Provides scientific leadership for the Downstream MSAT lab, supporting tech transfers and clinical/commercial processes in protein purification. Manages resource planning, project deadlines, and small-scale verification runs. Collaborates with SMEs, develops lab procedures, and supports investigations. Requires 3-4 years of experience in biopharmaceuticals, protein purification, and regulatory knowledge.

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.

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.

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.

Lead and develop a validation team in a regulated biopharma manufacturing environment. Plan and oversee validation lifecycle activities, manage deviations and change controls, and ensure timely, compliant execution.

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.

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 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.

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.

Senior Electronics Engineer will own electronics design from concept to production for next-generation analytical instruments. Lead development of analog and digital electronics, define design requirements, and collaborate with multidisciplinary teams.

Product Safety Specialist will act as a Subject Matter Expert in Product Safety, Low Voltage Directive, Machinery Directive/Regulation, and Technical Documentation. Responsibilities include monitoring global legislation, developing internal governance processes, supporting product development projects, and ensuring CE marking compliance. Requires a master's degree in a relevant field and at least 5 years of experience in product compliance, regulatory affairs, electrical safety, certification, or risk & safety.

Student Assistant to support project management, internal communication, and commercial topics within FOSS Go, a strategic initiative focused on digital-first commercial models.