57 English-speaking jobs in Hillerød

Are you passionate about qualifying advanced automated test systems? Do you enjoy ensuring that cutting-edge medical devices are tested with accuracy, reliability, and quality? Join us in shaping the future of drug delivery by enabling trusted design verification testing.

# Student Assistant - Project Management and CommunicationAnsøg hos virksomheden## JobbeskrivelseAre you passionate about engineering and project management and do you enjoy working in a global dynamic environment collaborating with a wide range of stakeholders, this may be the perfect position for you!

About the role In this temporary role, you will lead the area strategy and CI portfolio, tightly aligned with site priorities. You will plan and facilitate strategic workshops, build capability and leadership behaviors, and enable teams to run improvement initiatives.

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

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.

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.

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.

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.

Support the establishment and coordination of an AI community, connecting stakeholders and translating AI opportunities into practical value. Coordinate community events, maintain communication channels, and track community activities. Assist with documentation and contribute to shaping AI coordination across the organization.

This internship supports the development and coordination of a growing AI community within Global Contract Manufacturing Devices. The role involves planning and executing community events, maintaining communication channels, and facilitating collaboration across IT, business, and data domains.

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.

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.

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.

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.

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.

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