63 English-speaking jobs in Hillerød

Revenue Controller will join a dynamic Finance team and play a key role in controlling, delivering input to invoicing, and ensuring accurate and timely information for customers and stakeholders. Responsibilities include preparing invoice requests, payment requests, and invoice settlements, ensuring correct revenue recognition and reporting, and assisting in driving development and automation of contract-to-cash processes.

Business Process Owner for Quality Risk Management needed at Hillerød site. Oversee the Quality Risk Management Process, facilitate workshops and training, and present the area during audits and inspections. Requires a university degree in Natural Sciences and 2-4 years of experience with Quality Risk Management and GMP quality systems.

Senior Engineer I will lead global infrastructure delivery, support, and availability across compute, storage, networking, and platforms. Responsibilities include building, configuring, and optimizing enterprise technologies, driving cloud adoption, and ensuring security and compliance. Requires deep expertise in virtualization, cloud platforms, storage, backup/DR, networking, and security.

Leads the development and execution of site Quality Review Boards, working with operations and stakeholders to improve quality performance. Drives continuous improvement of governance, reporting, and action on quality signals. Facilitates training and support in the Quality Review Board process. Presents the site Quality Review Board process during audits and inspections.

Revenue Controller will join a newly established team and play a key role in controlling, delivering input to invoicing, and ensuring accurate and timely information to customers and stakeholders. Responsibilities include collecting and ensuring correct input for invoicing, preparing invoice requests and settlements, and ensuring correct revenue recognition and reporting.

Advanced Process Engineering Professional will support the installation, testing, and operation of robotic systems and automated equipment in a highly regulated production environment. Responsibilities include troubleshooting, maintenance, optimization, and preparing documentation.

Leads and evolves global hardware and software asset management capabilities across FLBG. Defines and executes the global IT Asset Management strategy, ensuring assets are optimized, compliant, and aligned with business goals. Leads global teams, governs asset lifecycle processes, and owns financial, vendor, and compliance accountability.

Leads and evolves global collaboration platforms, standards, and services across FUJIFILM Biotechnologies. Accountable for setting the global collaboration strategy, governing platform standards, and ensuring scalable, secure, and compliant collaboration services. Drives enterprise-wide collaboration transformation across Microsoft 365, Teams, SharePoint, OneDrive, Mobility, telephony, AV/meeting rooms, and digital productivity platforms.

Support onboarding of new products in the visual inspection area, performing manual and automated visual inspection. Assist in equipment/process qualification, validation, and studies. Participate in creating departmental procedures.

Experienced Senior Validation Engineer / Validation SME needed to drive validation activities for Cleanrooms, Classified Environments, and Clean Utilities. Responsibilities include technical ownership of the validation program, acting as SME during audits, and leading validation activities including IQ, OQ, PQ, and Continued Lifecycle Verification. Requires a Bachelor's, Master's, or equivalent degree in a relevant field and extensive experience qualifying and maintaining HVAC Systems, Cleanrooms, Clean Air Devices, and Clean Utilities. 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 is essential.

Provide support for daily production challenges in a 24/7 manufacturing environment. Troubleshoot issues, analyze production data, and drive corrective actions. Collaborate with production teams and stakeholders to ensure operational continuity and adherence to plans.

Senior QA for QC Specialist provides quality oversight to the QC laboratory. Responsibilities include reviewing and approving documentation, assessing changes and deviations, and ensuring adherence to procedures. The ideal candidate has 10+ years of experience in biologics manufacturing and is knowledgeable about GxP guidance and quality systems.

This role involves hands-on operation, troubleshooting, and optimization of robotic systems and automated process equipment in a highly regulated production environment. Responsibilities include supporting commissioning, verification, and validation activities, preparing maintenance strategies, and acting as a point of contact for operators during equipment issues.

Senior Researcher position at CAMES, Copenhagen. Develop and lead research focused on simulation-based and workplace learning, team performance, and interprofessional collaborative practice. Requires a primary medical or health-professional qualification, a research doctorate, and a strong international research track record.

Leads and evolves global hardware and software asset management capabilities across FLBG. Defines and executes the global IT Asset Management strategy, ensuring assets are optimized, compliant, and aligned with business goals. Leads global teams, governs asset lifecycle processes, and owns financial, vendor, and compliance accountability.

Leads and evolves global collaboration platforms, standards, and services across FUJIFILM Biotechnologies. Accountable for setting the global Collaboration strategy, governing platform standards, and ensuring scalable, secure, and compliant collaboration services. Drives enterprise-wide collaboration transformation across Microsoft 365, Teams, SharePoint, OneDrive, Mobility, telephony, AV/meeting rooms, and digital productivity platforms.

Leads global End User Computing (EUC) strategy, standards, and services across FUJIFILM Biotechnologies. Accountable for setting global EUC strategy, governing engineering standards, and ensuring scalable, secure, and compliant endpoint services. Drives enterprise-wide EUC transformation, modern endpoint management, and automation.

Support onboarding of new products in visual inspection, initially manual and transitioning to automated. Perform visual inspection for ongoing production and document tasks according to GMP. Assist with equipment/process qualification, validation, and studies. Contribute to development of departmental procedures.

Senior/Principal QC Scientist to support HPLC method lifecycle, troubleshooting, tech transfers, and junior staff coaching in a GMP setting. Experience with Waters systems, Empower software, antibody methods (e.g., SEC, Titer/PepMap), and LIMS required.

Lead a team of operators in a drug substance production environment, focusing on daily planning, task prioritization, and workflow optimization. Drive GMP standards, collaborate with cross-functional teams, and ensure smooth column packing operations.