102 English-speaking jobs in Hillerød

Develop and sustain CI systems and tools, coach on ideal behavior, lead improvement work, and train leaders and employees in lean tools and systems. Support leadership team with annual must-win battles and drive projects across Drug Substance Manufacturing. Represent the Drug Substance Organization in the company and collaborate with support functions.

Drive and coordinate QC change controls, collaborating with stakeholders and experts. Manage QC change records, engage with colleagues and partners, and document changes to quality processes.

Team Lead for both Upstream and Downstream QA teams supporting Drug Substance facility operations from Tech Transfer to product release. Focus on process, equipment, and digitalization. Lead, motivate, and prioritize tasks for the team, support team development, and represent the team in cross-functional collaborations.

Validation Engineer needed to support equipment and system validation in a growing biologics manufacturing facility. Responsibilities include commissioning, IQ, OQ, PQ activities, change controls, and cleaning validation. Requires a Bachelor's degree in Engineering or related field and 3+ years of industry experience. Strong technical writing and communication skills are essential.

Tech Transfer Lead will lead and manage technology transfer projects from development to commercialization. Responsibilities include creating project plans, managing communication, and ensuring compliance with regulatory requirements. Requires a Bachelor's or Master's degree and 5+ years of experience in technology transfer, process development, or manufacturing.

Automation Process Owner for Drug Product Manufacturing will design, implement, and maintain automation strategies for D.P.M equipment and systems. Responsibilities include leading automation workstreams for tech transfers, acting as a subject matter expert for IT-related projects, and ensuring the validated state of D.P. IT systems.

Provide high-quality accounting and administrative support for daily accounting operations. Work closely with finance colleagues and stakeholders. Responsibilities include accounts payable and receivable, intercompany invoicing and reconciliations, investment accounting, and bank and balance sheet reconciliations.

Production Operator needed for assembly, testing, and operation of heavy machinery at Cembrane's Danish facility.

Student Assistant to support Commercial and Technical departments. Collaborate with global sales and internal teams to deliver customer solutions. Explain technical concepts clearly and assist in preparing documentation.

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.

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

Coordinate method transfer activities across QC laboratories, customer relations, and contract organizations. Lead meetings to prioritize method transfers and develop transfer plans.

Facility Professional will manage outsourced services and act as an advisor on building expansion projects. Responsibilities include implementing changes within the architecture package, driving project coordination, and ensuring compliance with GMP standards. Requires a building construction education, minimum 3 years GMP experience, and fluency in English.

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

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.

As an Inventory Supporter, you ensure smooth production by managing material flow, coordinating projects, and supporting operators.

Designs, implements, and maintains the automation strategy for Drug Product Manufacturing (D.P.M) equipment and systems. Leads automation workstreams for tech transfers and harmonizes standards. Acts as Subject Matter Expert (SME) for IT-related projects and GMP events.

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.

Student Assistant position in QC Sample Control supporting Drug Substance, Drug Product, and Stability samples. Responsibilities include sample handling, aliquoting, inspections, and equipment cleaning.