62 English-speaking jobs in Hillerød

Experienced Site Quality Review Board Manager needed to build and mature quality governance across the site. This role requires expertise in GMP quality systems, cross-functional forums, and driving process improvements.

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

Lead the site finance agenda as VP, Head of Finance, partnering with leadership to drive growth and operational excellence. Ensure robust financial governance, transparent reporting, and team development within a complex environment.

Experienced Business Process Owner for Quality Risk Management to build QRM competence across the Hillerød site. Responsibilities include establishing governance, facilitating workshops, and ensuring system compliance. Requires a degree in Natural Sciences and 7+ years in QRM and GMP systems.

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 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.

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.

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.

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. 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.

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.

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.

Own end-to-end HR reporting and analytics for People & Culture, setting standards across Workday and Tableau. Design scalable data models, dashboards, and governance to fuel strategic business decisions. Requires 8+ years in HR analytics and 3+ years in Workday reporting.

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.

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.