49 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 and part-time professor position in physiotherapy at Copenhagen University Hospital – North Zealand and the Faculty of Health and Medical Sciences, University of Copenhagen. Applicants must be a board-certified registered physiotherapist with a PhD and experience in research on physical activity and exercise training for chronic diseases.

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.

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 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.

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.

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.

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.

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.

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.

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.

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.

Senior Supply Chain Project Manager to develop and improve supply chain processes, systems, and technologies. Drive the execution of supply chain strategy, ensuring a reliable and agile end-to-end supply chain.