Senior Associate, GMP Technician, Global Clinical Drug Supply

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.

Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.

Does this inspire you and feel like a fit? Then we would love to have you join us!

The Role

Genmab is looking for two dedicated Senior Associate GMP Technicians to join our new clinical secondary packaging and labelling facility in Ballerup, which is currently under establishment. In this role, you will be part of a small, agile team driving the rapid start-up of our clinical trials, with a particular focus on first-in-human (FIH) and early-phase studies. You will help ensure that high-quality investigational medicinal products reach patients with cancer and other serious diseases on time and in full.

As Genmab's first in-house GMP production capability for secondary packaging and labelling, this position offers a unique opportunity to help shape our ways of working from the very beginning. You will be responsible for secondary packaging, labelling, and related GMP activities in a small-scale, manual set-up, where your contribution will have a direct impact on timelines and quality.

The role combines hands-on production work with ownership of equipment maintenance, documentation, and continuous improvement across end-to-end production and facility-related processes.

• Perform secondary packaging and labelling activities for clinical trials according to approved batch documentation and GMP, including manual set-up and operation, in-process checks and reconciliations, and timely, accurate completion of batch documentation and logbooks
• Carry out label set-up and printing using validated systems and templates, ensuring labels are created and printed according to approved texts and design layouts
• Support the creation and maintenance of Master Batch Records and packaging instructions for secondary packaging and labelling activities by providing practical input
• Assist with equipment-related tasks in the packaging and labelling area, such as operation, cleaning and basic maintenance, and support qualification, calibration and validation activities under guidance
• Highlight and help troubleshoot equipment issues to support minimal downtime in a fast-paced environment
• Follow and contribute to SOPs, work instructions and checklists, and ensure all activities are performed in accordance with GMP, GDP and Genmab's quality system, including data integrity principles
• Support the handling of deviations, change controls and CAPAs within your area by providing accurate operational details and participating in implementation of agreed actions
• Participate in preparations for audits and inspections by ensuring your own area is inspection-ready and documentation is up to date
• Perform inventory and material management for labels, packaging materials and relevant consumables, including receipt, storage, issuance, reconciliation and stock checks
• Handle waste management from packaging and labelling operations, including segregation, documentation and disposal in line with SOPs, safety and environmental requirements
• Contribute to the practical set-up of new clinical trials, with focus on first-in-human and early-phase trials, by following instructions, being flexible and raising potential issues that may impact packaging timelines or product availability
• Participate in continuous improvement activities within the packaging and labelling area by sharing observations, suggesting practical improvements and helping to implement agreed changes

• Vocational education within pharmaceutical production, laboratory technology, process technology or a similar technical field; a Bachelor's degree in a relevant area is an advantage but not required
• 3+ years of experience from a GMP-regulated environment (e.g. pharmaceutical production, clinical packaging, aseptic/solid dose manufacturing or similar)
• Hands-on, technical mindset with the ability to operate equipment and learn basic maintenance under guidance, and to quickly learn new systems and tools
• Experience with label printing systems, cold storage equipment or clinical trial materials is an advantage but not a requirement
• Experience from a small-scale or start-up-like facility based on manual processes is considered a plus
• Basic understanding of GMP principles and documentation practices, and willingness to develop further in this area with high attention to detail and quality
• Proficient in English (written and spoken); Danish is an advantage
• Good IT skills and willingness to learn and use new digital tools and systems

• You are genuinely passionate about our purpose
• You bring precision and excellence to all that you do
• You believe in our rooted-in-science approach to problem-solving
• You are a generous collaborator who can work in teams with a broad spectrum of backgrounds
• You take pride in enabling the best work of others on the team
• You can grapple with the unknown and be innovative
• You have experience working in a fast-growing, dynamic company (or a strong desire to)
• You work hard and are not afraid to have a little fun while you do so!