45 English-speaking jobs in Hillerød

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.

We are looking for a warehouse a assistant for a temporary position at a tire center in Hillerød. There is a vacancy for a full-time temporary position starting this coming Monday until December 18th. Working Hours / Arbejdstid: Monday to Thursday / Mandag til torsdag: 07:30 – 16:30 Friday / Fredag: 07:30 – 14:30 (Early weekend!

Advanced Test Engineer to plan, execute, and document design verification for medical devices and primary packaging. Requires a relevant engineering degree and experience in testing within product development projects.

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.

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.

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.

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.

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.

Build secure development into FOSS software for analytical instruments and the IQX cloud platform. Own static/composition analysis, cloud security posture, and vulnerability triage. Requires software engineering background and application security knowledge.

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.

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.

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.

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.

Senior IT Systems Analyst for QC Applications manages Labware LIMS and Empower operations. Responsibilities include system maintenance, vendor coordination, and driving optimization projects while ensuring GxP compliance.

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.

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.

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.

Support Quality & Compliance in a fast-paced production environment. Responsibilities include handling deviations, performing shopfloor walks, and maintaining SOP accuracy, requiring cGMP experience.