111 English-speaking jobs in Hillerød

Drive and improve the material intake process, collaborating with stakeholders across QC, Material/Process Science, Supply Chain, and Purchasing. Identify process improvements, implement changes, and ensure visibility for all stakeholders.

Deliver exceptional guest experiences, ensure product quality, and maintain hygiene standards. Foster a positive work environment, demonstrate dedication, and adhere to company policies and procedures.

Automation Process Owner for Drug Product Manufacturing will design, implement, and maintain automation strategies for D.P.M equipment and systems. Responsibilities include acting as Work Package Owner for automation in tech transfers, serving as a subject matter expert for IT-related projects, and liaising with the U.S. site to harmonize systems and standards.

The Product Owner will develop and manage products, ensuring they meet client needs and align with company strategy. Responsibilities include performing product CQAs, leading process gap assessments, and owning product risk assessments. The ideal candidate has a minimum of 5 years of product management experience, preferably in pharmaceuticals, and strong project management and communication skills.

Leads and executes device stability studies to ensure product performance and compliance. Performs trending and data evaluation in LIMS, ensuring accurate documentation. Handles test results, including OOS/OOT investigations. Prepares and maintains protocols, reports, and documentation. Drives implementation of new processes and improvements within stability and quality control areas. Collaborates with cross-functional teams and utilizes digital tools to support a paperless laboratory workflow.

Experienced Tech Transfer Lead to manage technology transfer projects from development to commercialization for pharmaceutical clients.

Mechanical Quantity Surveyor needed for a data center project in Sweden. Manage cost control for mechanical works, including HVAC, cooling systems, and other infrastructure. Requires a degree in Quantity Surveying, Mechanical Engineering, or related field and 5+ years of experience.

Intern to support Global People & Culture strategy, planning, and execution. Responsibilities include portfolio management, communication, meeting coordination, process improvement, and change management. Must be enrolled in a relevant university program and have strong organizational, communication, and data analysis skills.

As an Inventory Supporter, you ensure smooth production by managing materials flow, coordinating projects, and supporting operators. You will work with SAP, KANBAN, and process improvements.

Student Assistant for the Quality Control Sample Control team will support a dynamic team in the handling of Drug Substance, Drug Product, and Stability samples. Tasks include sample collection, handling, aliquoting, and equipment cleaning. The position requires a detail-oriented individual currently enrolled in a university program studying biotechnology, chemistry, or microbiology. Fluent English is required.

Provide first line support for instrument breakdowns, generate GMP documentation, and coordinate instrument maintenance with vendors and stakeholders.

Support onboarding of new products in the visual inspection area. Perform manual inspection activities and documentation. Assist with equipment/process qualification, validation, and studies.

Support data analytics, market insights, and business development projects. Automate data workflows, develop data sources, and visualize insights. Participate in AI model experiments and contribute to data process improvements.

Supports onboarding of new products in the visual inspection area, performing manual and automated visual inspection. Assists in equipment/process qualification, validation, and studies. Participates in creating departmental procedures. Requires experience in visual inspection or aseptic drug product manufacturing and GMP understanding.

Facility Professional to advise partners on building expansion projects. Manage outsourced services and act as a change owner for GMP and non-GMP projects. Requires 3+ years GMP experience and fluency in English.

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. Drives a strong safety culture and fosters a high-performing team. Collaborates with cross-functional teams to ensure alignment and resolve complex issues.

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.

Intern will support Global People & Culture strategic initiatives, including portfolio management, communication, meeting coordination, process improvement, and change management activities.

Support onboarding of new products in the visual inspection area. Perform manual inspection activities and documentation. Assist with equipment/process qualification, validation, and studies.

Support data analytics, market insights, and business development projects. Automate workflows using Alteryx and Snowflake. Visualize insights with Tableau.