51 English-speaking jobs in Hillerød

Senior Project Manager will develop and improve supply chain processes, systems, and technologies to ensure a reliable and agile end-to-end supply chain. The role involves executing strategy, conducting process mapping, and driving projects to deliver on commitments.

Lead a newly established Operation Support team providing first-line support to the Drug Substance Manufacturing (DSM) floor. Build the team structure, priorities, and ways of working to ensure safe, compliant, and efficient 24/7 production. Drive issue resolution, remove obstacles, and collaborate with Production Leaders, Value Stream Directors, and cross-functional partners.

Leads rotating day and night shifts, overseeing 24-30 Manufacturing Associates. Ensures seamless production operation and models exemplary behavior, including teamwork, GMP adherence, productivity, and professionalism.

Production Leader oversees rotating day and night shifts, managing a team of 24-30 Manufacturing Associates. The role ensures seamless production operations, adherence to GMP, and high productivity.

Leads the development, optimization, and management of internal communication channels and applications, including the intranet, digital content tools, and collaboration platforms. Develops and implements a long-term strategy for internal communication platforms, ensuring alignment with business goals and employee needs. Provides advisory services to departments on their internal communications agendas. Collaborates with IT, Content, and Social Media teams to ensure consistent messaging and user experience. Supports Quarterly Business Updates and Quarterly Leadership Updates.

Senior Validation Engineer / Validation SME needed for Cleanrooms, Classified Environments, and Clean Utilities. Requires 15+ years of experience in HVAC/Cleanroom and Clean Utility GMP validation within pharmaceutical, biotechnology, or life science industries. Deep knowledge of EU GMP Annex 1, EU GMP Annex 15, ICH Q8/Q9/Q10, ISPE Guidance, ISO 14644, ASTM E2500, GAMP Principles, FDA regulations, and regulatory requirements.

Manages internal communication channels and applications, including the intranet, digital content tools, and collaboration platforms. Develops and implements internal communication strategies aligned with business goals and employee needs. Collaborates with IT, content, and social media teams to ensure consistent messaging and user experience. Provides training and support to departments on internal communication tools and best practices.

Senior Supply Chain Project Manager to develop and improve supply chain processes, systems, and technologies. Drive the execution of supply chain strategy, ensuring a reliable and agile end-to-end supply chain.

A clinical position as consultant of Neurology at Copenhagen University Hospital – Rigshospitalet is open. This position is combined with a 10-year clinical professorship (chair) of Neurology at the Faculty of Health and Medical Sciences, University of Copenhagen. Applicants must be board-certified specialist in Neurology and accepted for both positions.

Leads and drives ServiceNow deliverables end-to-end, ensuring business needs are met through stakeholder management and communication. Partners with the ServiceNow team to build and drive the ServiceNow roadmap. Responsible for 2nd level support, documentation, and configuration tasks. Drives smaller deployment or upgrade projects and participates in larger IT and compliance projects. Manages customer expectations and provides a single point of contact for IT systems.

Own end-to-end HR reporting and analytics for People & Culture, designing scalable reporting, data models, integrations, and dashboards across Workday, Tableau, and related systems. Define and govern HR reporting standards and KPI frameworks, ensuring consistent metrics and data lineage. Build, optimize, and maintain Workday reports and dashboards, and create Tableau dashboards and analytics solutions. Translate business questions into actionable insights and operate the intake and prioritization process for reporting requests.

Lead, coach, and develop a validation team, overseeing commissioning and qualification, cleaning validation, and periodic reviews. Manage validation schedules, protocols, and reports, ensuring timely completion and compliance.

Student Assistant to provide first- and second-line IT support, device setup, and collaboration tool assistance. Will handle IT tickets, support end-user devices and Microsoft 365 tools, and contribute to small IT projects. Must be enrolled in a relevant Bachelor's or Master's program and have strong communication skills.

Lead and develop teams of operators in Filling and Formulation within a Drug Product Manufacturing facility. Manage team growth, competencies, and cross-collaboration. Ensure on-time delivery per customer agreements and uphold cGMP compliance.

Lead and manage the strategic vision for the bioreactor scale-up team. Develop and execute methodologies for scaling cell culture processes from bench top to large scale bioreactors. Serve as the primary point of contact for customers regarding scaling processes.

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

As a Validation Engineer, you will prepare, execute, and finalize validation protocols for equipment and processes, ensuring regulatory compliance. You will investigate deviations, drive CAPAs, and mentor junior staff.

Senior Validation Engineer / Validation SME needed for Cleanrooms, Classified Environments, and Clean Utilities. Drive validation activities, including VPP, Commissioning & Quality Assurance Strategies, IQ, OQ, PQ, and Continued Lifecycle Verification. Extensive experience qualifying and maintaining HVAC Systems, Cleanrooms, Clean Air Devices, and Clean Utilities required. Strong knowledge of EU GMP Annex 1, EU GMP Annex 15, ICH Q8/Q9/Q10, ISPE Guidance, ISO 14644, ASTM E2500, GAMP Principles, FDA regulations, and regulatory requirements.

Laboratory Technician needed for QC Chemistry department. Responsibilities include chemical testing of samples, method transfer, troubleshooting, and maintaining a cGMP laboratory. Requires 4+ years of experience in the pharmaceutical industry, knowledge of GMP and quality systems, and experience with various chemistry methods. Fluency in English is required.

Leads and drives ServiceNow deliverables end-to-end, managing operations and maintenance of the platform. Partners with the ServiceNow team to build and drive the roadmap, ensuring business needs are met. Provides 2nd level support and documentation for ServiceNow. Drives smaller deployment or upgrade projects and participates in larger IT and compliance projects. Requires 5-10 years of experience managing systems, preferably in the pharmaceutical industry.