34 English-speaking jobs in Hillerød

Senior Systems Engineer needed for early-stage development projects. Requires a mechanical engineering background with experience in pen injectors or drug delivery systems. Responsibilities include leading systems engineering, requirements definition, and risk analysis.

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

Full-time 3-year position assisting AI researchers with image analysis and data processing at DEPICT. Requires strong programming skills, Linux experience, and prior Deep Learning model development experience.

Implement and operate the ISO 27001:2022-certified ISMS, driving control implementation across business units. Validate controls, support audits, and maintain documentation. Requires knowledge of ISO 27001/27002 and professional English.

Implement and operate the ISO 27001:2022-certified ISMS, driving control implementation across business units. Validate controls, support audits, and maintain documentation. Requires knowledge of ISO 27001/27002 and professional English.

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.

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.

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.

R&D Director for Grain & Feed oversees all NPD projects, managing the core team. This role requires leading cross-functional projects spanning engineering, software, and data science to bring innovative analytical solutions to market.

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.

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.

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.

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.

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.