56 English-speaking jobs in Hillerød

Senior Associate in Pharmaceutical Quality System (PQS) ensures product quality standards. Responsibilities include leading customer audits and regulatory inspections, managing CAPAs, and maintaining PQS compliance with ICH Q10/Q9 and EU GMP. Requires 5-7+ years in GxP industries.

Experienced Project Planner needed for a 12-month contract on a major pharmaceutical capital investment programme. Requires 10+ years in large-scale CAPEX, strong Primavera P6 skills, and experience in regulated industries.

Support communication, project management, and innovation activities. Responsibilities include creating materials, maintaining SharePoint sites, and coordinating events. Requires strong analytical skills and proficiency in English.

Support communication, project management, and innovation activities. Responsibilities include creating materials, maintaining SharePoint sites, and coordinating events. Requires relevant university enrollment and strong analytical skills.

Product Development Professional to shape safe medical devices. Drive risk management (ISO 14971), develop system requirements, and support design control across the product lifecycle. Requires technical background and experience in regulated environments.

Student Assistant for the Global Commercial Team providing administrative and office support to executives. Requires enrollment in a relevant Bachelor's or Master's program and strong organizational skills.

This temporary 2-year role supports system-level product development for medical devices. Responsibilities include driving risk management, developing system requirements, and supporting verification and validation activities.

Student Assistant to provide administrative and office support to the Chief Business Officer, Senior Vice President, and Commercial Leadership Team. Responsibilities include travel arrangements, expense report processing, and other administrative duties. Must be enrolled in a Danish educational program with at least two years of study remaining.

Own the end-to-end HR reporting and analytics capability for the People & Culture function. Design, build, and maintain scalable reporting, data models, integrations, and dashboards across Workday, Tableau, and related systems. Translate business questions into actionable analytics and insights.

Student assistant to support internal and external communications for a Danish manufacturing site. Responsibilities include content creation, social media support, and administrative tasks. Must be a student studying communication, digital media, journalism, marketing, or a related field.

Senior Infrastructure Engineer to lead global infrastructure availability, scalability, and security across data centers and cloud. Build, configure, and optimize enterprise technologies including VMware, Windows Server, Citrix, Linux, and storage platforms. Drive cloud adoption on AWS and/or Azure. Translate architectural designs into operational solutions and champion information security controls.

Leads sales enablement strategy, operating model, and global team. Experience in sales enablement, commercial excellence, or sales coaching required. Strong program/project management and instructional design skills. Familiarity with CRM, content platforms, LMS, and analytics tools. Excellent communication and presentation skills.

Leads sales enablement strategy, operating model, and global team. Experience in enterprise sales cycles, biopharma services, and sales enablement tools. Strong instructional design, commercial operations, and communication skills.

Lead the global growth of FOSS' Inside Sales channel, driving sales performance and business growth across subsidiaries. Manage sales training programs and facilitate meetings with subsidiaries and distributors.

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

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.

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.

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.

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.

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.