46 English-speaking jobs in Hillerød

Set the global vision for facilities, engineering standards, maintenance excellence, and asset lifecycle strategy. Lead network-wide engineering, calibration, and maintenance activities to drive reliability and operational performance in a regulated environment.

The CQV Permit Office Manager controls permit-to-work, LOTO, and safety governance during complex construction commissioning. This role ensures structured, compliant execution, acting as the interface between construction completion and operational readiness.

Commissioning Manager to oversee post-construction commissioning for complex projects. This role requires strong understanding of RAMS, LOTO, and HSE to coordinate activities safely and ensure operational readiness.

Three-year Postdoctoral Position in CRISPR-Based Genome Editing. Develop patient-tailored CRISPR therapy for Glanzmann thrombasthenia, focusing on translational workflow and preclinical assessment. Requires PhD and strong CRISPR/cell biology experience.

Architect and scale a world-class global procurement function for a CDMO. Lead strategy, build teams, and drive value across quality, cost, and risk for critical direct materials. Requires 12+ years of sourcing experience in pharma/biotech under cGMP/GxP.

Experienced CQV professional needed for a contract role supporting Drug Product validation. Responsibilities include developing re-validation strategies, providing technical oversight for re-validation activities, and coordinating cross-functional stakeholders in a GMP environment.

Experienced CQV Consultant needed to lead the development of a Master Validation Plan for a Drug Product programme. This contract role requires 10+ years of Drug Product experience in GMP environments, focusing on equipment, process, and technology transfer validation.

Principal Cloud Infrastructure Engineer leads IT/OT Cloud roadmaps and provides technical strategy for mission-critical cloud infrastructure. This role designs, builds, and maintains global cloud services, ensuring security, reliability, and availability.

Architect and scale a world-class global procurement function for a CDMO. Set strategy, build the team, and drive value across quality, cost, and risk for critical materials. Requires 12+ years of experience in pharma/biotech under cGMP/GxP.

Mid-level SRE to own and mature platform observability and alerting. Responsibilities include designing alert conditions in New Relic, building monitoring tooling, and collaborating on SLIs/SLOs. Requires 3-5 years of SRE experience and Python scripting skills.

Sales Enablement Lead to build the enablement engine for a global sales organization. This role bridges Marketing and Sales, owning content governance and building the enablement platform. Requires B2B sales/enablement experience.

Senior QA Associate provides quality oversight for Materials, Supply Chain, and Warehouse operations, focusing on material qualification and new material onboarding for GMP manufacturing. This role requires 7+ years in pharma/biotech with strong GMP knowledge.

Sales Enablement Lead to build the enablement engine for a global sales organization. This role bridges Marketing and Sales, owning content governance and building the enablement platform and tech stack. Requires B2B sales/enablement experience.

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.

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 improvement across the site.

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.

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.

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.

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.