48 English-speaking jobs in Hillerød

Senior QA Associate to support Drug Product Manufacturing operations. Manage deviations, CAPAs, change controls, and risk assessments. 5+ years QA experience in pharmaceutical industry required.

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

Senior researcher position in physiotherapy at Copenhagen University Hospital – North Zealand combined with a part-time professorship at the University of Copenhagen. Applicants must be a board-certified registered physiotherapist with a PhD and experience in quantitative research methods, physical activity research, and chronic disease treatment.

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.

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.

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

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.

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.

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.

Experienced consultants, engineers, or project managers sought for freelance opportunities in pharma, biotech, or manufacturing. Work on impactful projects with a network of top professionals.

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.

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.

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.

Leads the development, optimization, and management of internal communication channels and applications, including the intranet, digital content tools, and collaboration platforms. Develops and implements a long-term strategy for internal communication platforms, ensuring alignment with business goals and employee needs. Provides advisory services to departments on their internal communications agendas. Collaborates with IT, Content, and Social Media teams to ensure consistent messaging and user experience. Supports Quarterly Business Updates and Quarterly Leadership Updates.

Senior Validation Engineer / Validation SME needed for Cleanrooms, Classified Environments, and Clean Utilities. Requires 15+ years of experience in HVAC/Cleanroom and Clean Utility GMP validation within pharmaceutical, biotechnology, or life science industries. Deep knowledge of EU GMP Annex 1, EU GMP Annex 15, ICH Q8/Q9/Q10, ISPE Guidance, ISO 14644, ASTM E2500, GAMP Principles, FDA regulations, and regulatory requirements.

Manages internal communication channels and applications, including the intranet, digital content tools, and collaboration platforms. Develops and implements internal communication strategies aligned with business goals and employee needs. Collaborates with IT, content, and social media teams to ensure consistent messaging and user experience. Provides training and support to departments on internal communication tools and best practices.