80 English-speaking jobs in Hillerød

Experienced Quality Assurance professional will serve as the primary point of contact for customers regarding quality-related topics during commercial and Tech Transfer processes.

QA Specialist to perform reviews, manage incidents, handle deviations, and lead CAPA processes. Requires 5+ years of QA/validation experience, including documentation review, incident management, and deviation handling.

This 12-month contract position supports IT Systems and Computerized Equipment management. Responsibilities include assisting with life cycle management, supporting compliance documentation, and acting as a technical resource during projects. The ideal candidate has a bachelor's degree in a related field and 2-3 years of experience in IT System/Computerized Equipment Management.

Support Vice President and leadership team in setting strategic agenda, planning priorities, and preparing for meetings. Assist with budget tracking, financial reporting, and coordinating cross-functional initiatives. Provide executive support including calendar management, travel arrangements, and communication.

This role oversees the governance, lifecycle, and deployment of a global DCS and MES library across manufacturing sites in Denmark and the United States. Responsibilities include ensuring version alignment, driving standardization, and enabling efficient and compliant deployment. The Global Library Manager will also monitor versions, plan upgrades, design migration strategies, and coordinate stakeholders.

Temporary Product Development Engineer to lead risk management activities for manual pre-filled syringe products. Collaborate with cross-functional partners to ensure regulatory compliance and high-quality decision-making throughout the product lifecycle.

This 12-month contract position supports IT governance and compliance for IT Systems and Computerized Equipment within Sourcing Operations. Responsibilities include assisting with life cycle management, maintaining compliance documentation, and acting as a technical resource during projects.

Leads and manages a team of manufacturing associates across day and night shifts in upstream drug substance manufacturing. Coordinates with shift teams to ensure smooth operations and resolves issues. Implements systems and processes to manage emergencies and minimize downtime.

Manage the full lifecycle of IT systems, including documentation, validation, compliance, and risk assessments. Support business operations through incident handling, escalations, and collaboration with production and engineering teams. Act as the main liaison for suppliers and service partners. Drive system changes and upgrades.

Manage the full lifecycle of IT systems supporting production processes. Responsibilities include documentation, validation, compliance, patch management, and risk assessments. Support business operations through incident handling, escalations, and collaboration with production and engineering teams.

Security Systems Specialist to own and manage validated and non-validated security systems, ensuring compliance, performance, and integration. Responsible for system strategy, delivery, and day-to-day reliability, including change and configuration management, auditability, and regulatory compliance.

Lab Scientist will plan, coordinate, and analyze cell culture processes for upscaling from small to large scale. Responsibilities include assessing and improving lab practices, authoring technical documentation, and collaborating with clients and stakeholders. Requires a PhD or M.Sc. in a relevant field with 3-5 years of industrial experience in cell culture development and scale-up.

Supports the Vice President and leadership team in setting strategic priorities, preparing materials for meetings, and tracking initiatives. Provides financial support including budget tracking and reporting. Manages the VP's calendar, coordinates meetings, and handles travel arrangements.

Leads and manages a team of manufacturing associates across day and night shifts in upstream drug substance manufacturing. Implements systems and processes to manage emergencies and minimize downtime. Fosters a strong safety culture and prioritizes growth through training and development. Collaborates with cross-functional teams to ensure smooth operations.

This role oversees the governance, lifecycle, and deployment of a global DCS and MES library across manufacturing sites in Denmark and the United States. Responsibilities include ensuring version alignment, driving standardization, and enabling efficient deployment. The Global Library Manager will design and execute migration strategies, build standardized migration packages, and coordinate stakeholders across Manufacturing, Engineering, and QA.

Experienced Release Train Engineer (RTE) & Transformation Lead to drive and scale lean-agile delivery across MES and automation. Establish and mature a lean-agile operating model, facilitate agile ceremonies, and optimize flow using Kanban, WIP limits, and data-driven improvements. Manage cross-team dependencies, risks, and impediments in a global, matrixed setup. Coach Scrum Masters, Tech Leads, Product Owners, and teams in agile/SAFe, DevOps, and built-in quality. Monitor and communicate delivery metrics to stakeholders and leadership.

Drive and scale lean-agile delivery across a global MES and automation landscape. Establish and mature a lean-agile operating model tailored for MES and automation in a regulated (GxP) environment. Facilitate agile ceremonies, optimize flow, and integrate change control into delivery processes. Coach teams in agile/SAFe, DevOps, and built-in quality. Manage cross-team dependencies, risks, and impediments in a global, matrixed setup.

Senior SAP Supporter will build a reliable SAP PM/MM foundation for maintenance and calibration in a new GMP production facility. Responsibilities include setting standards, structuring equipment and spare parts data, and ensuring smooth process operations.

Act as a safety risk manager, taking ownership of end-to-end risk management for manual pre-filled syringe products. Collaborate with cross-functional partners to ensure robust documentation, regulatory compliance, and high-quality decision-making throughout the product lifecycle.

Experienced Continuous Improvement Partner to accelerate performance in Drug Substance Manufacturing. Coach teams in Lean and PDCA/A3, lead Kaizen, and embed Shingo-aligned behaviors to improve cycle time, quality, waste, and cost in a cGMP environment.