43 English-speaking jobs in Hillerød

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.

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.

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.

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.

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.

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 during turnover, commissioning, and CQV. Responsibilities include coordinating daily RAMS, facilitating risk assessments, and ensuring safe execution of activities.

Senior Secondary Packaging Engineer responsible for maintaining and improving the global secondary packaging portfolio. Duties include driving design verification, providing expert input on quality issues, and supporting global production sites. Requires a Master's degree and regulated industry experience.

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 and drive ServiceNow deliverables end-to-end, managing platform operations and global adoption. Partner to build the roadmap, handle 2nd level support, and perform configuration tasks.

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

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.

Lead the Bioreactor Scale-Up team, setting global vision using expertise in cell culture process modeling and simulation. Drive projects from bench to production scale while serving as a primary customer contact.

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.

Architect the digital backbone for FLBG manufacturing by translating business needs into scalable, GxP-compliant architectures connecting shop floor to cloud. Ensure security and reliability across IT/OT systems.

Manage and validate PLM, CAD, and CAE systems like CATIA and Windchill for Drug Delivery Innovation. This role involves system administration, project delivery, user support, and ensuring compliance.