56 English-speaking jobs in Hillerød

Structured Manufacturing Expert needed for Operations Support. Troubleshoot issues, drive root-cause analysis, and coordinate cross-functionally to ensure smooth 24/7 production. Requires downstream manufacturing experience and data-savvy problem-solving skills.

Senior researcher position in physiotherapy at Copenhagen University Hospital – North Zealand combined with a part-time professorship at the University of Copenhagen. Applicants must be a board-certified registered physiotherapist with a PhD and experience in quantitative research methods, physical activity research, and chronic disease treatment.

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.

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.

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 quality mindset improvements.

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 role ensuring product quality via Pharmaceutical Quality System (PQS). Lead/support customer audits and regulatory inspections, manage CAPAs, and maintain PQS compliance with ICH Q10/Q9 and EU GMP. Requires 5-7+ years in GxP industries.

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 (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.

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.

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.

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.

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.

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.

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

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.