70 English-speaking jobs in Hillerød

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.

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.

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.

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.

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.

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.

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.

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.

Lead a team of 10 in Column Pack operations, optimizing workflows, driving GMP standards, and ensuring smooth cross-functional collaboration.

Supports onboarding of new products in visual inspection, performing manual and automated inspection activities. Documents tasks and assists with equipment/process qualification and validation.

Leads and evolves global collaboration platforms, standards, and services across FUJIFILM Biotechnologies. Defines and owns the global collaboration strategy, governs platform architecture, and ensures optimal user experience. Drives enterprise-wide collaboration transformation across Microsoft365, Teams, SharePoint, OneDrive, mobility, telephony, AV/meeting rooms, and digital productivity platforms.

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.

Validation Engineer needed for temporary position (end date 31.03.27) at FUJIFILM Biotechnologys Denmark. Prepare, execute, and finalize validation protocols for new and modified glasswashers. Experience with cleaning validation and glasswasher PQ in a GMP-regulated biotech/biopharma environment required.

Experienced Quality Assurance professional needed to serve as primary customer contact for quality-related topics during commercial and Tech Transfer processes. Drive discussions with customers on deviations, changes, CAPAs, and complaints. Support manufacturing activities and represent quality assurance in program core teams.

Experienced Quality Assurance professional will serve as the primary point of contact for customers regarding quality-related topics during commercial and Tech Transfer processes. The role involves driving discussions with customers on deviations, changes, CAPAs, and complaints.

Validation Engineer needed for temporary position (ending 31.03.27) to execute and finalize validation protocols for new and modified glasswashers. Experience with cleaning validation and glasswasher PQ in a GMP-regulated environment required.

Leads a team of service technicians, ensuring safety compliance, performance targets, and quality standards. Manages workflow, training, and communication within the service center. Requires a technical automotive background, strong leadership skills, and proficiency in English.

Lead and develop clinical translation within the Clinical Epidemiological Research section at Steno Diabetes Center Copenhagen. Manage a team of 15-20 employees focused on developing, conducting, and translating epidemiological research into improved prevention and treatment of diabetes and cardiometabolic diseases.