36 English-speaking jobs in Hillerød

Automation Engineer needed to program, develop, and validate automation systems, specializing in Emerson DeltaV. Responsibilities include system design, troubleshooting, and providing technical support within the pharmaceutical industry. A relevant engineering degree is required.

Lead a senior team to ensure flawless execution of technology transfer projects into large-scale manufacturing. Own strategy, governance, and cross-functional alignment for new program introductions.

Three-year Postdoctoral Position in CRISPR-Based Genome Editing. Develop patient-tailored CRISPR therapy for Glanzmann thrombasthenia, spanning genetic characterization, model development, and safety assessment in stem cells. Requires PhD and strong CRISPR/cell biology experience.

Architect and scale a world-class global procurement function for a CDMO. Drive supply assurance, TCO optimization, and strategic supplier management across direct materials while ensuring cGMP/GxP compliance.

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 responsible for planning and governing post-construction commissioning activities on complex projects. Requires strong understanding of RAMS, LOTO, and HSE to ensure safe execution and transition to 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.

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.

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.

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.

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.

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.

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.

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.

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 (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 technical integrity. This role leads lifecycle management and supports cross-functional teams.

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.