Research Associate, GLP QA Support at Genmab · Utrecht

Research Associate, GLP QA Support Location: Utrecht 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 currently seeking a dedicated and detail-oriented Research Associate (QA Support) for a temporary 6-month. This entry-level role offers a unique opportunity to gain experience in Quality Assurance (QA) within a biotech environment. The selected candidate will play a key role in supporting Good Laboratory Practice (GLP)/ Good Clinical Laboratory Practice (GCLP) Proactive  audits at our Utrecht location and will receive on-site training to ensure a smooth transition into the role. This is an excellent opportunity for someone looking to develop their expertise in QA and gain hands-on experience with industry-standard systems and processes. Responsibilities Provide operational support for QA-related activities, particularly in relation to GLP/GCLP audits. Work with Veeva GenDocs, managing backend processes and supporting system maintenance. Assist in creating and managing templates/forms within the GenDocs system. Once trained, approve minor extension requests related to QA processes. Collaborate with internal teams to ensure compliance with GLP/GCLP guidelines. Support the overall efficiency of QA operations and documentation management. Requirements Bachelor's degree in Life Sciences, Biotechnology, or a related field. Prior experience in QA is not required; on-the-job training will be provided. Strong organizational skills and keen attention to detail. Ability to learn and adapt quickly in a fast-paced environment. Experience with document management systems (e.g., GenDocs) is a plus. Excellent communication and collaboration skills. Availability to start as soon as possible. This is a temporary position for 6 months, with the possibility of extension depending on business needs. About You 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! Locations Genmab maximizes the efficiency of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are crafted as open, community-based spaces that work to connect employees while being immersed in our powerful laboratories. Whether you’re in one of our office spaces or working remotely, we thrive on connecting with each other to innovate. About Genmab Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab’s vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines. Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X. Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website Job Applicant Privacy Notice (genmab.com). Please note that if you are applying for a position in the Netherlands, Genmab’s policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the contract.