46 English-speaking jobs in Hillerød

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

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

Experienced CQV Consultant needed to lead the development of a Master Validation Plan for a Drug Product programme. This hands-on contract role requires expertise in equipment and process validation within GMP environments.

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

R&D Director for Grain & Feed oversees all NPD projects, managing the core team. Requires experience leading cross-functional projects in mechanical engineering, electronics, software, and data science.

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.

Senior/Principal QC Scientist needed for HPLC in Biologics/Antibodies. Focus on method lifecycle, troubleshooting, and tech transfers in a GMP setting. Requires hands-on pharma/biologics QC experience.

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.

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 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 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.

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.

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.

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.