63 English-speaking jobs in Hillerød

Business Technology & Digital Solutions is a rapidly growing organization driving digital transformation at FUJIFILM Biotechnologies. As part of the End User Services/ Global Digital Workplace within Infrastructure & Operations (I&O), this role plays a critical part in ensuring stable, efficient, and compliant IT services globally.

And do you have experience from Visual Inspection and/or other aspects of aseptic drug product manufacturing combined with solid GMP understanding? Then we hope you will join us soon! Your New RoleYou'll support the onboarding of new products in the visual inspection area, initially focusing on manual visual inspection and transitioning to automated visual inspection.

Business Technology & Digital Solutions is a rapidly growing organization driving digital transformation at FUJIFILM Biotechnologies. As part of the End User Services / Global Digital Workplace within Infrastructure & Operations (I&O), this role plays a critical part in ensuring stable, efficient, secure, and compliant Collaboration services globally.

Advanced Process Engineering Professional for state‑of‑the‑art API facility Location: Hillerød, Capital Region of Denmark, DK Are you passionate about working with advanced process equipment and robotics in a highly automated production environment?

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.

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.

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.

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 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.

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.

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.

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.

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.