61 English-speaking jobs in Hillerød

Develop primary packaging systems for oral and parenteral products. Translate regulatory and quality requirements into engineering solutions. Prepare technical documentation and collaborate with stakeholders. Requires an Engineering or Pharmacy degree and 5+ years of relevant experience.

Lead Product Development Engineer for primary packaging systems for oral and parenteral drug delivery. This role involves technical development, regulatory compliance, and leading cross-functional projects. Requires an MSc/BSc in Engineering or Pharmacy with 7+ years of relevant experience.

Senior Product Development Engineer maintains and improves marketed medical devices, focusing on risk management, design control, and technical integrity. Responsibilities include leading life cycle management and supporting post-market activities.

Advanced Validation Engineer responsible for qualifying and validating automated test systems for medical devices. Leads equipment acquisition, maintenance, and documentation in a regulated environment. Requires technical background and experience with design verification testing.

Associate Manager, CI & Projects for maternity cover. Lead CI strategy, portfolio management, and drive change within QA DS Operations using lean methods. Requires 3+ years in pharma/biopharma GMP environment.

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.

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.

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 relevant university enrollment and strong analytical 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 coordination and development of the GCMD AI community. Coordinate events, maintain community channels, and enable collaboration. Create engaging materials, promote AI initiatives, and track community activities. Assist with documentation and contribute to shaping AI governance.

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 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.

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.

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.

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