53 English-speaking jobs in Hillerød

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.

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.

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.

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.

Laboratory Technician performs cGMP-compliant analytical testing, method development, and laboratory operations. Experience with a range of chemistry methods, including HPLC/CE-SDS/cIEF testing, is required.

Lead the end-to-end transfer, optimization, and implementation of downstream processes into a manufacturing facility. Translate process knowledge into scalable, compliant, and efficient operations, steering activities from new product introduction to validation and continuous improvement.

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 a self-service reporting ecosystem. Design and deliver Tableau dashboards and analytics solutions, translating business questions into actionable insights. Manage reporting requests, set SLAs, and communicate timelines. Coordinate the Employee Satisfaction survey program and partner with HRIS and IT on integrations and defect remediation.

Lead a team of experienced TT Leads, ensuring role clarity, delivery discipline, and psychological safety. Build and maintain the TT portfolio overview, including capacity planning, resource allocation, and prioritization. Drive effective governance, stage gates, risk/issue escalation, and milestone tracking. Ensure cross-functional alignment with Manufacturing, MSAT/Process Development, QA/Regulatory, Supply Chain, QC, and customers. Oversee integrated project plans and support CMC activities, including inputs to regulatory filings and inspection readiness.

Senior IT Systems Analyst to manage Labware LIMS and Empower systems, ensuring operational excellence, compliance, and continuous improvement. Requires 15+ years of IT experience, pharmaceutical industry knowledge, and strong analytical and problem-solving skills.

Leads and drives ServiceNow deliverables end-to-end, owns platform operations and maintenance, and champions global adoption. Partners with the ServiceNow team to build and execute the platform roadmap, aligning with Core Functions strategy. Provides 2nd level support, manages small deployments and upgrades, and ensures business needs are met through stakeholder management and communication.

Senior IT Systems Analyst for QC Applications will manage and maintain Labware LIMS and Empower systems, ensuring business operations improvement, compliance, and vendor coordination. Requires 15+ years of IT experience, including pharmaceutical industry knowledge, Labware LIMS and Empower administration, and project management.

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.

Clinical consultant position in paediatrics at Copenhagen University Hospital – Herlev and Gentofte combined with a 5-year clinical professorship in paediatrics with a focus on sleep in neuropaediatric patients at the University of Copenhagen. Applicants must be board-certified specialists in Paediatrics with documentation for subspecialisation in paediatric neurology.

Leads and manages the strategic vision for the scale-up team, aligning with global scale-up teams to ensure unified strategies. Develops and executes methodologies for scaling cell culture processes from bench top to large scale bioreactors. Serves as the primary point of contact to customers regarding scaling of their processes.

Laboratory Technician needed for QC Chemistry department. Will perform chemical testing of samples, participate in method transfers and improvement projects, and maintain a cGMP laboratory. Requires 4+ years experience in the pharmaceutical industry, knowledge of GMP and quality systems, and experience with various chemistry methods. Fluency in English is required.

Laboratory Technician to drive and support stability studies, procedures, and projects. Responsibilities include authoring protocols, managing stability studies, and compiling data reports. Requires a strong quality mindset, GMP knowledge, and excellent communication skills.

Lead a team of operators in Filling and Formulation lines within Drug Product Manufacturing. Manage team growth, development, and performance to meet production goals. Ensure compliance with cGMP and quality standards.

Leads a team of 30+ Manufacturing Associates (MAs)/Operators in the Drug Substance Manufacturing Department. Responsibilities include fostering team development, providing shop-floor leadership, identifying process improvements, and ensuring compliance with cGMP regulations. Requires proven experience leading diverse teams in a production environment, knowledge of pharmaceutical manufacturing activities, and experience with LEAN and/or Shingo principles. Must be able to work a fixed day-shift schedule, including every other weekend and some evenings/nights.

As a Validation Engineer, you will prepare, execute, and finalize validation protocols for equipment and processes, ensuring compliance with regulatory expectations. You will investigate deviations, drive root cause analysis, and prevent recurrence across sites. You will also mentor junior staff and oversee contractors.