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!

REQUIREMENTS:

• It is expected that you have a master’s degree in natural science, pharmacy, or similar. Preferable a Ph.D.
• You have at least 5 years of documented professional experience with analytical methods in a GMP QC setting
• You have a thorough understanding of the detailed requirements for analytical validation and are up to date with current trends
• You have active and recent experience within analytical development and validation of methods for biologics/monoclonal antibodies from a phase II/III program
• You have experience with ELISA´s and pharmacopeia methods for biologics. Experience with other analytical methods is also desirable

THE ROLE & DEPARTMENT

As a Senior Scientist you will be a part of QC in the BioAssay team. Joining our QC team in Ballerup, you will play a key role in the establishment of the laboratory which includes and is not limited to: Method transfers, Validation of Analytical methods, authoring and reviewing laboratory procedures, and supporting qualification of new analytical instruments.
You will report to the Team Manager and work closely with Scientist within QC and our development site in Utrecht.

KEY RESPONSIBILITIES INCLUDE:

• Play a key role in establishing the new QC laboratory.
• Conduct method transfers from our development laboratory in Utrecht
• Perform validation of analytical methods.
• Author and review laboratory procedures.
• Support qualification of new analytical instruments.