Project Manager, Life Cycle Management

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! About the Role Genmab is seeking a Project Manager CMC Product Lifecycle Management to

• join the CMC Life Cycle Management (LCM) Team and support our growing portfolio of commercial products globally.

The LCM team is responsible for managing the CMC lifecycle activities of Genmab’s commercial products and manufacturing oversight, ensuring supply continuity, regulatory compliance, and successful execution of post-approval activities throughout the product lifecycle. In this role, you’ll work closely with LCM Product Lead and colleagues across Commercial Supply Chain, MSAT, Regulatory CMC, Commercial QA and External Manufacturing to ensure seamless execution of lifecycle management activities. The CMC Life Cycle Management Team is part of CMC Project & Portfolio Management (PPM) which also includes the Early-Stage Development, Late-stage Development and External Manufacturing teams. CMC Project & Portfolio Management resides within CMC Development and Manufacturing, based in Denmark. This role offers a unique opportunity to contribute to the continued growth of Genmab's commercial portfolio while working in a highly collaborative and cross-functional environment at the interface of development, manufacturing, supply, and regulatory affairs. Responsibilities

• Work alongside the LCM Lead to provide manufacturing oversight and execute lifecycle activities for an assigned manufacturing track (DS, BI, CI or DP) after commercial launch, supporting batch release and reliable supply. The LCM Lead retains overall product accountability.
• Lead operational governance with internal functions and partners/CMOs, aligning priorities, preparing decisions, tracking progress and actions, and providing input on CMO performance.
• Collaborate with internal and external stakeholders on daily operations to ensure manufacturing oversight (ie. Deviation management, change control, complaint handling, etc) , support batch release and supply, issues resolution/escalation and quality/regulatory compliance.
• Coordinate technical issue resolution and manage track risks with relevant experts, ensuring required assessments, documentation and mitigation actions, and escalating issues with proposed next steps.
• Drive manufacturing changes, projects and improvements within agreed scope, timelines and budgets.
• Support implementation of CMC commitments and Post-approval change management related to assigned product manufacturing track (i.e DS, BI, CI, DP) and support coordination of submission documentation preparation across stakeholders and CMOs/Partners.
• Support initiatives to optimize yield, reduce cost of goods, and enhance robustness of manufacturing and testing processes
• Help establish and improve LCM processes, governance, tools and ways of working, incorporating lessons learned.

Requirements

• Master's degree in science or related technical discipline (e.g. engineering, biotech, pharmaceutical, biochemistry, biology) or equivalent experience;
• 4+ years of experience in biopharmaceutical industry, preferably within manufacturing operations, lifecycle, product management for commercial products.
• Experience in building relations and influencing multi-functional teams within multicultural organizations.
• Proven track record in CMC project management, manufacturing operations management or product management across development and commercialization activities.
• Experience managing and defining project coordination activities and tasks in a structured, regulated environment.
• Prior experience with commercial product lifecycle management and oversight of Contract Manufacturing Organizations (CMOs) is considered an advantage.
• Broad understanding of global cGMP requirements and regulatory expectations across major markets
• Excellent communication and stakeholder management skills, with fluency in English
• Demonstrated ability to work effectively in cross-functional and multicultural environments
• Strong organizational skills with the ability to manage multiple priorities, balance competing demands, and deliver against project timelines
• Team player with the ability to collaborate with diverse stakeholders.
• Result- and goal-oriented, committed to contributing to Genmab’s success

The proposed gross annual/hourly base salary range for this position, in the primary location, based on a full time schedule is: DKK597.312,00-895.968,00 The final salary offer will depend on several factors, including your skills, qualifications, and experience. In addition to base salary, this position is eligible for 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 eligibility for compensation and benefits based on the role 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).