61 English-speaking jobs in Hillerød

Scientist to manage OOS/OOT investigations, deviation investigations, and CAPAs in a QC Compliance team. Experience in cGMP and pharmaceutical manufacturing preferred.

Leads sales enablement strategy, operating model, and global team. Experience in biopharma services, CDMO, GxP environments preferred. Strong program/project management and executive communication skills.

Business Process Owner for Quality Risk Management will oversee the Quality Risk Management Process, facilitate workshops and training, and present the area and process during audits and inspections.

Site Quality Review Board Manager will establish and mature site governance for Quality Review Boards, ensuring continuous improvement. The role will facilitate site Quality Review Boards that provide guidance, solve issues, and support a quality mindset. The manager will shape the site Review Board structure, processes, and ways of working in partnership with operations and stakeholders.

Drive global growth of FOSS' service business by leading commercial development and operations of the Inside Sales channel. Manage sales training programs, drive sales performance, and communicate with subsidiaries and distributors.

Drive end-to-end Process Excellence and Global Transformation at FOSS. Support Global Process Owners in developing and maturing end-to-end processes including Record-to-Report, Hire-to-Retire, and Source-to-Pay. Facilitate workshops to define governance, roles, standards, and ways of working. Create transparency across processes, systems, roles, and data ownership. Identify opportunities for harmonization, simplification, and continuous improvement. Partner with Master Data and IT to align processes, data, and enterprise systems.

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.

Business Process Owner for Quality Risk Management will oversee the Quality Risk Management Process, facilitate workshops and training, and ensure the system supports customer requirements. Requires a university degree in Natural Sciences, 2-4 years of experience with Quality Risk Management, and GMP quality systems.

Site Quality Review Board Manager will establish and mature site governance for Quality Review Boards, ensuring continuous improvement. The role provides guidance and support to operations related to quality governance and overview, ensuring Review Boards create value for operations.

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.

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.

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.