41 English-speaking jobs in Hillerød

Postdoctoral Bioinformatician role bridging functional genomics and clinical population genetics. Lead CRISPR screen analysis and large-scale human genetic studies on biobank data. Requires PhD and expertise in high-throughput sequencing and genetic epidemiology.

Validation Engineer needed for the Downstream team. Responsibilities include writing/reviewing IQ, OQ, PQ protocols, participating in PPQs, and executing cleaning validation. Requires a Bachelor's degree and 3-5 years of industry experience.

Strategic leader to shape policy and drive results in Drug Product, Finished Goods, and Tech Transfer Engineering. Focus on improving equipment performance and developing necessary structures. Requires 6+ years of management experience.

Seeking a Warehouse Assistant for a temporary, full-time position at a tire center. Duties include handling, sorting, and moving tires, plus general warehouse tasks. Must be physically fit, reliable, and speak Danish or English.

Job category Product & Portfolio Strategy – Device Verification Development Job Description Location Hillerød, Denmark Job category Product & Portfolio Strategy – Device Verification Development Product & Portfolio Strategy | Device Verification Development Hillerød, Denmark | 12-Month Fixed-Term Contract Your impact begins here As an Advanced Test Engineer, you will plan, execute and docume

Validation Engineer needed for the Downstream team. Participate in PPQs, capex changes, and audits. Write/review IQ, OQ, PQ protocols and manage cleaning validation. Requires 3-5 years of industry experience.

Experienced Risk Coordinator needed for a pharmaceutical project supporting turnover, commissioning, and CQV. Responsibilities include coordinating daily RAMS, conducting risk assessments, and ensuring safe execution of activities.

Advanced Product Development Engineer role focusing on medical device development and lifecycle management. Requires an engineering degree and experience in regulated environments. Responsibilities include technical issue investigation and cross-functional collaboration.

Own the full lifecycle of design verification and shelf-life testing for medical device and packaging projects. Lead testing, author protocols, and analyze data to ensure products meet requirements. Requires an Engineering degree and experience in testing.

Project Manager to lead analytical method transfer activities in a GMP Quality Control environment. This role coordinates cross-functional teams to ensure method transfers meet quality and compliance standards. Requires a relevant degree and experience in pharma/biotech method transfer.

Lead R&D team developing core optical and spectroscopic technologies, including NIR, LIBS, and computer vision. Requires technical background in optics/spectroscopy/vision, strong people management, and product development experience.

Senior Product Development Engineer develops primary packaging systems for parenteral products. This role translates regulatory and quality requirements into engineering solutions, managing technical documentation and stakeholder collaboration. Candidates need relevant experience in primary packaging development.

Senior Secondary Packaging Engineer ensures robust, compliant, and sustainable global packaging solutions. Responsibilities include driving design verification, supporting production, and managing lifecycle improvements. A Master's degree in a relevant science is required.

Sales Support & Business Development Specialist supports the Indirect Sales team by managing distributor and customer activities. This role involves coordinating commercial documentation, identifying new business opportunities, and building product knowledge.

Student Assistant - Digitalization Drug Delivery Innovation - Process Excellence & Digitalization Your new role As a Student Assistant in Digitalization, you will support daily activities, documentation, project coordination and practical tasks related to IT systems and digital ways of working.

Experienced Risk Coordinator needed for a pharmaceutical project during turnover, commissioning, and CQV. Responsibilities include coordinating daily RAMS, facilitating risk assessments, and ensuring safe execution of activities.

Experienced Risk Coordinator needed for a pharmaceutical project supporting turnover, commissioning, and CQV. Responsibilities include coordinating daily RAMS, conducting risk assessments, and ensuring safe execution of activities.

Lead a senior team to set direction and ensure flawless execution of technology transfer projects into large-scale manufacturing. Own strategy, planning, and execution while standardizing best practices.

Experienced Validation Engineer/SME needed for Controlled Temperature Units (CTUs) like refrigerators. Drive validation strategy, ensure regulatory compliance, and lead IQ/OQ/RQ activities within the life science industry.

Lead end-to-end drug substance tech transfer into large-scale manufacturing. Drive compliant introduction of clinical, PPQ, and commercial processes, partnering with internal teams and customers. Requires 8+ years in CMC process development/GMP.