62 English-speaking jobs in Hillerød

Validation Engineer needed for temporary position (ending 31.03.2027). Prepare, execute, and finalize validation protocols for equipment and processes. Investigate deviations, drive CAPA, and ensure compliance with regulatory expectations. Lead cross-site validation improvements and mentor junior staff.

Lead and develop teams of operators in Filling and Formulation within a Drug Product Manufacturing facility. Ensure cGMP compliance, quality, and a safe work environment. Manage team growth, competencies, and cross-collaboration.

Lead a team of nine Investigators overseeing deviations for a single API production line (cell culture through purification). Optimize the deviation process, reduce lead time, and strengthen quality and audit readiness while maintaining GMP compliance.

Internship opportunity in Drug Substance Manufacturing focusing on process optimization, data analysis, and LEAN methodologies. Interns will support improvement initiatives, analyze data, and contribute to projects enhancing efficiency.

Lead a team of 30+ Manufacturing Associates in Drug Substance Manufacturing. Provide shop-floor leadership, training, and development. Drive continuous improvement and problem-solving. Experience in pharmaceutical manufacturing and LEAN principles required.

Product Safety Specialist will act as a Subject Matter Expert in Product Safety, Low Voltage Directive, Machinery Directive/Regulation, and Technical Documentation. Responsibilities include monitoring global legislation, developing internal governance processes, supporting product development projects, and ensuring CE marking compliance. Requires a master's degree in a relevant field and at least 5 years of experience in product compliance, regulatory affairs, electrical safety, certification, or risk & safety.

Student Assistant to support project management, internal communication, and commercial topics within FOSS Go, a strategic initiative focused on digital-first commercial models.

Senior Electronics Engineer will own electronics design from concept to production for next-generation analytical instruments. Lead development of analog and digital electronics, define design requirements, and collaborate with multidisciplinary teams.

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.

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.

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.

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.

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.

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.

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.

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.

Leads rotating day and night shifts, overseeing 24-30 Manufacturing Associates. Ensures seamless production operation and models exemplary behavior, including teamwork, GMP adherence, productivity, and professionalism.

Production Leader oversees rotating day and night shifts, managing a team of 24-30 Manufacturing Associates. The role ensures seamless production operations, adherence to GMP, and high productivity.