64 English-speaking jobs in Hillerød

Laboratory Technician to drive and support stability studies, procedures, and projects within the Stability team. Responsibilities include authoring and maintaining stability protocols, managing stability studies, and compiling stability data reports. Requires experience in the pharmaceutical industry, knowledge of stability requirements, and strong GMP Quality Systems understanding.

Support ongoing work at the Drug Product MSAT departments, driving small technical activities related to equipment in aseptic production. Contribute to projects, understand GMP environments, and develop and support colleagues.

Student Assistant to provide first- and second-line IT support, device setup, and collaboration tool assistance. Responsibilities include handling support tickets, configuring devices, and supporting Microsoft 365 tools. Must be enrolled in a relevant Bachelor's or Master's program.

Lead a team of nine Investigators overseeing deviations for a single end-to-end API line (cell culture through purification). Optimize deviation process, reduce lead time, and strengthen right-first-time quality and audit readiness. Collaborate with Manufacturing, QA, MSAT, Engineering, and Customers.

Student assistant for the Validation Support Equipment team. Support validation engineers during testing by assisting with preparations and maintaining loggers. Organize loggers, calibration sheets, and work orders. Perform LIMS label creation and support PQ/RQ testing.

Student Assistant to support sustainability initiatives, focusing on Scope 3 emissions, supplier engagement, and process optimization. Collaborate across functions and sites, turning data into insights and supporting initiatives that reduce environmental impact.

Internship in Manufacturing Sciences and Technology – Drug Product supporting aseptic production equipment activities. Tasks include measuring plunger insertion, providing input to work instructions, and handling inspection samples.

Leads and manages the strategic vision for the bioreactor scale-up team. Develops and executes methodologies for scaling cell culture processes from bench-top to large-scale bioreactors. Serves as the primary point of contact for customers regarding process scaling.

Lead and develop a validation team in a regulated biopharma manufacturing environment. Plan and oversee validation lifecycle activities, manage deviations and change controls, and ensure timely, compliant execution.

Leads risk-based validation activities for Drug Product and Finished Goods, including equipment, processes, utilities, and computerized systems. Prepares and executes validation protocols and documentation. Acts as a Validation Subject Matter Expert, defining strategies and ensuring compliance with global standards.

Senior Validation Engineer / Validation SME needed for Cleanrooms, Classified Environments, and Clean Utilities. Requires deep technical expertise, regulatory knowledge, and experience with qualification and validation activities in GMP environments.

Leads a new Operation Support team providing 24/7 support to Drug Substance Manufacturing, ensuring safe, compliant, and efficient production. Drives issue resolution, removes obstacles, and ensures seamless production execution through collaboration with Production Leaders, Value Stream Directors, and cross-functional partners.

Lead and develop a team of nine Investigators, managing workload and ensuring high-quality investigations and CAPAs across cell culture through purification. Drive standard work, visual management, and performance metrics. Optimize handovers and escalation paths with Manufacturing and QA. Promote cross-training and continuous improvement initiatives.

As a Student Assistant in Finished Goods Manufacturing, you will support interns, manage KPIs, perform production analyses, and optimize processes. You will collaborate with production, management, and QA.

Validation Engineer needed for temporary position ending March 31, 2027. Prepares, executes, and finalizes validation protocols and reports for equipment and processes. Investigates deviations, conducts root-cause analysis, and drives CAPA implementation. Requires 3-5 years of validation/qualification experience, preferably including cleaning validation. Strong understanding of regulatory requirements and guidance. Excellent cross-functional collaboration and communication skills.

As the Senior Reporting & Analytics Process Owner, you will design, build, and maintain HR reporting and analytics capabilities across Workday, Tableau, and related systems. You will define and govern HR reporting standards, KPI frameworks, and data governance, ensuring a single, trusted source of workforce truth. You will translate business questions into actionable insights and empower stakeholders through training and data literacy initiatives.

Intern for QA Drug Substance Manufacturing will support Continuous Improvement (CI) initiatives in QA DS. Responsibilities include mapping processes, presenting data-driven solutions, engaging with stakeholders, and developing KPIs. Applicants should be pursuing a degree in manufacturing or production engineering and have a basic understanding of industrial problem-solving methods.

Lead and execute risk-based validation across Drug Product and Finished Goods, covering equipment, processes, utilities, and computerized systems. Prepare/execute VPP/VFR, IQ/OQ/PQ, AVP/AVR for new/modified equipment and utilities. Act as Validation SME, defining strategies, acceptance criteria, and lifecycle documentation aligned with site/global standards. Perform QMS activities in TrackWise, including investigations and effectiveness checks. Ensure ALCOA+ data integrity, inspection readiness, and support/lead FDA/EMA and customer audits.

Senior Project Manager will develop and improve supply chain processes, systems, and technologies to ensure a reliable and agile end-to-end supply chain. The role involves executing strategy, conducting process mapping, and driving projects to deliver on commitments.

Lead a newly established Operation Support team providing first-line support to the Drug Substance Manufacturing (DSM) floor. Build the team structure, priorities, and ways of working to ensure safe, compliant, and efficient 24/7 production. Drive issue resolution, remove obstacles, and collaborate with Production Leaders, Value Stream Directors, and cross-functional partners.