62 English-speaking jobs in Hillerød

Experienced Site Quality Review Board Manager needed to establish and mature site governance. This role requires expertise in GMP quality systems, cross-functional forums, and driving quality mindset improvement.

Develop primary packaging systems for oral and parenteral products. Translate regulatory and quality requirements into engineering solutions, preparing technical documentation and collaborating with stakeholders. Requires relevant experience in packaging development.

Lead Product Development Engineer for Oral & Vial primary packaging. Develop systems and components for oral/parenteral products, ensuring regulatory compliance and safety risk management. Requires 7+ years of relevant industry experience.

Senior Product Development Engineer maintains and improves marketed medical devices, focusing on risk management, design control, and change control. This role leads lifecycle management and supports cross-functional technical leadership.

Senior Product Development Engineer maintains and improves marketed medical devices, focusing on risk management, design control, and technical integrity. This role leads lifecycle management and supports cross-functional teams.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.