Manager, Commercial Supply Chain Planning

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

The Manager , Commercial Supply Chain Planning plays a key role in coordinating end-to-end product supply activities across Genmab’s global commercial and clinical supply chains. This role is responsible for planning, execution, and oversight of Contract Manufacturing Organization (CMO) activities, ensuring reliable and compliant product supply to markets including the EU, US, and Japan.

Acting as a primary interface with CMOs and cross-functional stakeholders, the position supports both daily operational supply chain activities and the development of a robust, GxP-compliant planning infrastructure. The role operates within a global, regulated environment and contributes directly to supply continuity, operational excellence, and Genmab’s mission to transform patient lives through innovative antibody medicines.

You will be joining the Commercial Supply Chain team reporting to Associate Director, Commercial Supply Chain. The team is responsible for Genmab’s global supply chain activities.

Key Responsibilities

As Manager , Commercial Supply Chain Planning you will be responsible for planning and executing supply chain activities across commercial and clinical programs, ensuring alignment between demand, manufacturing, and distribution.

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Oversee daily supply chain operations, including order management, replenishment, inventory planning, and forecasting across international markets

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Coordinate production planning and manufacturing activities for commercial and clinical products (Drug Substance, Drug Product, labeling and packaging) across EU, US, and Japan

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Act as key interface with CMOs to align on production schedules, execution, and supply priorities

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Serve as key user of ERP systems (e.g., SAP S/4HANA), supporting planning, execution, and data integrity

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Ensure GxP compliance across the supply chain in collaboration with Quality Assurance, including deviation handling, root cause analysis, and CAPA implementation

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Identify and mitigate supply risks to ensure continuity and business resilience

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Support audits, inspections, and regulatory compliance activities through proper documentation and process adherence

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Contribute to continuous improvement initiatives and support new product introductions and CMC project activities

Requirements

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Bachelor’s or Master’s degree in Supply Chain Management, Engineering, Business Administration, Life Sciences, or a related field

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+6 years of experience in supply chain planning, logistics, or a related function

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Experience within biotech, pharmaceutical, or other GxP-regulated industries is preferred

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Hands-on experience with ERP systems (e.g., SAP S/4HANA) and supply planning tools

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Strong analytical skills with experience in data analysis and forecasting (e.g., Excel, Power BI, or similar tools)

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Familiarity with global supply chain operations and Contract Manufacturing Organizations (CMOs) is an advantage

Moreover, you meet the following personal requirements

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Strong stakeholder management and cross-functional collaboration skills

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Solid written and verbal communication skills

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Strong organizational and multitasking abilities

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Ability to operate effectively in high-pressure, deadline-driven environments

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Advanced proficiency in ERP systems and planning platform

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Advanced user of Microsoft Office Suite

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Understanding of GMP/GDP requirements within regulated supply chains

The proposed gross annual base salary range for this position, in the primary location, based on a full time schedule is:

DKK584.000,00---876.000,00

The final salary offer will depend on several factors, including your skills, qualifications, and experience.

In addition to base salary, this position is eligible to additional forms of compensation, such as discretionary bonuses and long-term incentives.

When you join Genmab, you become a part of a culture that supports your physical, financial, social, and emotional well-being. Our benefits include, but are not limited to:

• Pension
• Health insurance and wellness benefits
• Paid time off
• Employee support programs

Further details on compensation and benefits will be provided during the recruitment process.

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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