60 English-speaking jobs in Hillerød

Product Safety Specialist needed to shape product compliance and regulatory affairs. Act as SME for Product Safety, Low Voltage/Machinery Directives, and technical documentation. Requires a Master's in engineering and 5+ years in product compliance.

Student Assistant supporting Communication in Denmark. Craft content for internal channels, shape social media, and support teams with technical topics. Requires strong English writing and attention to detail.

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

Manage and mature site governance for Quality Review Boards, ensuring continuous improvement and operational value. Facilitate boards, drive innovation, and support a strong quality mindset across the site.

Lead the site finance agenda as VP, Head of Finance, partnering with leadership to enable growth. Ensure robust financial governance, transparent performance management, and drive financial performance across the site.

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

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

Lead Product Development Engineer for Primary Packaging (Oral & Vial). Develop systems and components for oral/parenteral products, ensuring compliance and safety. Requires 7+ years experience in packaging development.

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 an MSc/BSc in Engineering or Pharmacy with 5+ years of relevant 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 collaborates cross-functionally.

Lead Product Development Engineer for primary packaging systems for oral and parenteral drug delivery. Requires 7+ years of experience in packaging development, regulatory compliance, and project leadership.

Develop primary packaging systems for oral and parenteral products. Translate regulatory and quality requirements into engineering solutions, preparing technical documentation. Requires an MSc/BSc in Engineering or Pharmacy with 5+ years of relevant experience.

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.

Support project management and communication for FPMSAT Packaging Engineering. Responsibilities include creating materials, maintaining SharePoint, and coordinating events. Requires relevant studies and strong analytical skills.

Advanced Validation Engineer to ensure design verification test equipment delivers reliable, compliant data. Lead qualification and validation of automated test systems, managing maintenance and documentation. Requires technical background and experience in regulated environments.

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

Product Development Professional to manage system engineering and risk management for medical devices. Responsibilities include driving ISO 14971 risk activities, developing requirements, and supporting V&V.

Senior Associate in Pharmaceutical Quality System ensures product quality standards. Responsibilities include leading customer and regulatory audits, 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 expertise in regulated industries.