Senior Manager, Commercial Supply Chain Planning

Genmab

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 Senior Manager, Commercial Supply Chain Planning has a critical role in leading end-to-end planning across Genmab’s global supply chains. This position is accountable for translating Forecast into integrated supply plans that ensure reliable, compliant, and timely product supply to commercial markets.

The role provides senior-level coordination of CMO capacity, production and supply priorities across Drug Substance, Drug Product, labeling, and pack activities. Acting as a key cross-functional partner to Supply Chain, Quality Assurance and External Manufacturing; the Senior Manager drives alignment on batch execution flow, capacity constraints, risk mitigation, and decision-making required to maintain supply continuity in a global GxP-regulated environment.

You will be joining the Commercial Supply Chain team reporting to the Associate Director, Commercial Supply Chain. The team is responsible for Genmab’s global supply chain activities and for ensuring robust, scalable, and compliant planning processes that support Genmab’s mission to transform patient lives through innovative antibody medicines.

Key Responsibilities

As Senior Manager, Commercial Supply Chain Planning, you will be responsible for leading end-to-end supply planning and execution across commercial and clinical programs, ensuring strong alignment between demand, manufacturing capacity, batch execution, quality release, and distribution requirements.

  • Lead end-to-end supply planning across the value chain, connecting demand, inventory, production, batch release, and distribution plans into one integrated supply view across markets and programs

  • Drive CMO capacity coordination, including capacity reviews, production slot planning, constraint identification, scenario planning, and prioritization of manufacturing activities across Drug Substance, Drug Product, labeling, and packaging

  • Coordinate batch execution flow between Supply Chain, Quality Assurance, MFG Life cycle Mgt, Logistics and CMOs to ensure clear ownership, timely handoffs, documentation readiness, deviation follow-up, release prioritization, and escalation of issues impacting supply

  • Act as the senior supply chain interface with CMOs and internal stakeholders, aligning production schedules, execution risks, batch status and supply priorities

  • Drive planning governance, performance tracking, and communication forums to support transparent decision-making across Supply Chain, QA and MFG Life cycle teams

  • Identify, assess, and mitigate supply and capacity risks, developing contingency plans that strengthen business resilience and protect patient supply

  • Serve as a senior key user and process owner for ERP and planning systems (e.g., SAP S/4HANA) and ANAPLAN ensuring planning discipline, master data accuracy, transaction quality, and data integrity

  • Ensure GxP compliance across supply chain planning and batch execution processes in collaboration with Quality Assurance, including support for deviation handling, root cause analysis, CAPA implementation, audits, and inspections

  • Contribute to continuous improvement initiatives, new product introductions, CMC project activities, and process standardization efforts that improve planning maturity, execution reliability, and scalability

Requirements

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

  • +8 years of experience in supply chain planning, external manufacturing, or a related function, preferably with experience in a senior planning or cross-functional coordination role

  • Experience within biotech, pharmaceutical, or another GxP-regulated industry is preferred

  • Strong understanding of end-to-end supply chain planning, including demand and supply balancing, capacity planning, production scheduling, inventory management, batch release flow, and distribution dependencies

  • Hands-on experience working with CMOs, including production planning, capacity coordination, operational governance, and issue escalation

  • Experience coordinating cross-functional batch execution activities involving Supply Chain, Quality Assurance, External Manufacturing, and/or CMC stakeholders

  • Hands-on experience with ERP systems (e.g., SAP S/4HANA) and supply planning tools, with a strong focus on planning discipline and data integrity

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

  • Solid understanding of GMP/GDP requirements within regulated supply chains and experience supporting audits, inspections, and compliance-driven processes

Moreover, you meet the following personal requirements:

  • Strong senior stakeholder management skills with the ability to influence across functions, geographies, and external partners

  • Excellent written and verbal communication skills, with the ability to translate complex planning, capacity, and batch execution topics into clear decisions and actions

  • Strong organizational and prioritization skills, with the ability to manage multiple programs, CMOs, and execution timelines in parallel

  • Ability to operate effectively in high-pressure, deadline-driven environments and to escalate risks with clarity and recommended mitigation options

  • Proactive, structured, and solution-oriented mindset with a continuous improvement focus

  • Advanced proficiency in ERP systems, planning platforms like ANAPLAN, and Microsoft Office Suite

  • High level of accountability, collaboration, and ownership for supply continuity and compliant execution



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

DKK640.000,00-960.000,00

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.



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).

Hvordan man ansøger

For at ansøge om dette job skal du autorisere på vores websted. Hvis du ikke har en konto endnu, bedes du tilmelde.