72 English-speaking jobs in Hillerød

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.

Lab Scientist to provide scientific leadership for Downstream MSAT lab, supporting tech transfers and clinical/commercial processes in protein purification.

Student Assistant will support the Downstream Process Engineering team with tasks such as creating material lists, updating documentation, and analyzing production data.

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 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 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.

Internship opportunity in Drug Substance Manufacturing focusing on process optimization, data analysis, and LEAN methodologies. Interns will support improvement initiatives, analyze data, and contribute to projects enhancing efficiency.

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 end-to-end API line (cell culture through purification). Optimize deviation process, reduce lead time, and strengthen right-first-time quality and audit readiness. Collaborate with Manufacturing, QA, MSAT, Engineering, and Customers.

Student Assistant to support sustainability initiatives, focusing on Scope 3 emissions, supplier engagement, and process optimization. Collaborate across functions and sites, turning data into insights and supporting initiatives that reduce environmental impact.

Support ongoing work at the Drug Product MSAT departments, driving small technical activities related to equipment in aseptic production. Contribute to projects, understand GMP environments, and develop and support colleagues.

Student Assistant to provide first- and second-line IT support, device setup, and collaboration tool assistance. Responsibilities include handling support tickets, configuring devices, and supporting Microsoft 365 tools. Must be enrolled in a relevant Bachelor's or Master's program.

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.

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.

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.

As a Student Assistant in Finished Goods Manufacturing, you will support interns, manage KPIs, perform production analyses, and optimize processes. You will collaborate with production, management, and QA.

As the Senior Reporting & Analytics Process Owner, you will design, build, and maintain HR reporting and analytics capabilities across Workday, Tableau, and related systems. You will define and govern HR reporting standards, KPI frameworks, and data governance, ensuring a single, trusted source of workforce truth. You will translate business questions into actionable insights and empower stakeholders through training and data literacy 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.