CMC Coordinator

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

Join Genmab as a CMC Coordinator

Are you ready to shape the future of science and medicine? At Genmab, our clinical pipeline is advancing rapidly-from First-in-Human studies to late-stage development and market approvals.
To support our expanding portfolio, we're strengthening our in-house laboratory capabilities, and we're looking for a passionate CMC Coordinator to bridge our projects and labs.

This is your opportunity to take on a pivotal new role at the heart of innovation in a company committed to improving the lives of people with cancer.

The role is based in as a split Copenhagen and Ballerup, Denmark, and offers a hybrid work environment.

Role & Department

You'll be part of the CMC New Product Introduction (NPI) department, which includes five specialized teams: three Project Management (PM) teams, a CMC Writer team, and a CMC Stability team.
The position sits within one of our PM teams and supports primarily early- but also late-stage development projects.

In this role, you'll collaborate closely with your colleagues, the CMC PM, the CMC project team, the Genmab science and technology department in Utrecht (S&T) and the Genmab QC laboratory.
Your coordination will be essential to keep our laboratory activities aligned with project timelines.

As this is a new position at Genmab, you'll have the opportunity to shape the role and define ways of working in supporting our projects.

Responsibilities

• Plan assay implementations, qualifications, validations, and start of release and stability testing within the QC laboratory.
• Coordinate QC project plans and tasks within the CMC Management team on behalf of CMC PM and QC assigned project scientists.
• Identify and escalate project risks or delays and help drive timely resolution. Participate in relevant CMC project teams to enable cross-project communication and coordination.
• Collaborate with Genmab CMC PMs, QC, QA, S&T and other departments to support the development projects.

Requirements

• A master's degree in a relevant scientific field.
• Minimum 5 years of experience in the biopharmaceutical industry.
• Proven track record in coordinating CMC activities within cross-functional environments.
• Strong understanding of antibodies and relevant analytical methods.
• Solid knowledge of CMC development for clinical-stage products.
• Able to work effectively and reliably under tight deadlines in a busy environment.
• Comfortable working with a wide range of people across different teams and organizations.
• Structured and systematic approach to tasks.
• Ability to manage multiple tasks, prioritize work, and define steps needed to achieve project and team goals.

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.

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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 fixed-term employment contract.