Supply Chain CoordinatorAPI Pilot PlantsBagsværd, Denmark, OnsiteYour new roleAs a Supply Chain Coordinator, you will be the operational backbone that ensures seamless material flow across our four API pilot plants. Your work directly enables the production of active pharmaceutical ingredients for clinical programmes that will one day reach patients worldwide.Day-to-day your tasks will include:
Coordinating end-to-end logistics solutions, including material flows, storage, staging, internal transportation, and cross-pilot transfersEnsuring alignment with production needs, quality requirements, safety standards, and operational workflowsCollaborating with stakeholders across Purification, Chemistry, Recovery, Freezing/Storage, QA, Tech Support, Facilities, Supply Chain, Procurement, and PlanningManaging raw materials, consumables, solvents, intermediates, and API containers to ensure readiness and availability at the right time and placePlanning, scheduling, and maintaining efficient and compliant operations during production campaignsDocumenting processes, flows, and system changes to ensure compliance with GMP and Good Documentation PracticeThis role is pivotal in maintaining flow and efficiency in a dynamic pilot-production environment, where strong coordination, standardisation, and a milestone-oriented mindset are essential.Your new departmentYou will join the Purification Pilot Plant department, which consists of 6 teams, including four pilot facilities located across two sites, a solvent production team, and a support team. We are part of the API Pilots organisation, responsible for producing active pharmaceutical ingredients for [xxxxx]'s clinical programmes. Specifically, you'll be part of our solvent team, which is currently expanding its responsibilities across the department. Our team is known for its collaborative spirit, dynamic environment, and commitment to delivering high-quality results.Your skills & qualificationsYou bring experience from complex pharmaceutical production environments and thrive in cross-functional, fast-moving pilot-plant settings. You are structured, proactive, and comfortable making decisions in a dynamic operation where priorities shift with campaign needs.We expect that you:Have a Master’s degree in Engineering, Life Sciences, Pharmacy, Biotechnology, Chemical Engineering, or a related fieldHave experience from API or pharmaceutical pilot-scale production, development manufacturing, or other GMP-regulated operations where material flow, readiness, and coordination are centralUnderstand logistics processes in a pilot-plant context, including handling of raw materials, solvents, intermediates, and API, as well as supporting equipment and staging workflowsHave experience with production planning and/or materials planning, preferably in environments where schedules depend on campaign execution and cross-facility coordinationAre familiar with SAP-based business processes (experience with PASX, STYX, SAP, EWM, WMS, or similar is an advantage) and can use digital systems to track, document, and maintain material flowsCan document processes, flows, and system changes clearly, ensuring compliance with GMP and Good Documentation PracticeCommunicate confidently with production teams, QA, warehouse, procurement, and technical support, and can facilitate coordination meetings or smaller workshopsWork analytically and independently, taking ownership of logistics tasks and keeping production supplied without interruptionAre detail-oriented and quality-focused, understanding the importance of traceability, timely documentation, and GMP complianceAre fluent in English, written and spoken (Danish is a plus but not required)On a personal level, you enjoy teamwork in a multi-pilot operational setup, thrive in multicultural and cross-disciplinary environments, and naturally create structure while simplifying and standardizing where possible.Working at [xxxxx]Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. Here, your contribution matters – whether you're coordinating materials for the next clinical trial or collaborating across teams to solve complex challenges. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.What we offerThere is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.DeadlineApril 26th – 2026We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At [xxxxx], we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Bagsværd.
Jobbet er oprettet på vores service den 14.4.2026, men kan have været deaktiveret og genaktiveret igen.
