EnglishWillDo

Specialist, Master Data Management

Genmab · Copenhagen, Denmark

No Danish requiredPosted yesterday
Apply for this job

You apply on the site where the job is posted. I never handle applications.

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

The Specialist, Master Data Management is responsible for ensuring the accuracy, consistency, and governance of critical business data across enterprise systems. This role supports operational excellence by maintaining timely and high-quality master data, driving continuous improvement initiatives, and partnering with stakeholders to enable efficient business processes and reliable reporting.

Responsibilities

  • Act as “Master Data Responsible” and maintain GxP and associated master data for all GxP materials in the Genmab ERP-system (SAP) and connected systems (like e.g. Tracelink).
  • Streamline and set standards for use of Master Data across multiple modules within ERP (SAP) such as Inventory Management, Contract Manufacturing, Supply Chain Management and Quality Assurance.
  • Establish and maintain supply chain master data in collaboration with Supply Chain, QA, RA, Finance and CMC.
  • Manage the setup, implementation, testing and validation of new product flows (Supply Chain Maps).
  • Participate in new systems setup/system enhancements as necessary.
  • Responsible for maintaining GxP compliance throughout the supply chain network related to master data management including exception handling – Investigate exceptions, determine root causes, implement CAPAs and drive closure in accordance with Genmab’s quality system.
  • Support the implementation of new technologies to help Supply Chain Management in daily operations.

Requirements

  • Bachelor’s or Master’s degree in a business or technical discipline (e.g., Business Economics, IT, Engineering, or a related field). Candidates with a Bachelor’s degree should demonstrate Master’s-level capabilities gained through professional experience. Advanced degrees or relevant certifications are an advantage.
  • 4+ years of experience in Master Data Management (MDM) or related area in relevant industry (e.g., biopharma, biotech, medical devices) or equivalent combination of education and experience.
  • Strong working knowledge within MDM area with ability to solve complex problems independently.
  • Strong understanding of GXP-regulated supply chains, experience in translating supply chain maps into required systems setup.
  • Proficiency in ERP systems and other supply chain tools, including data analysis and reporting.
  • Experience coordinating project activities, aligning work with organizational priorities, and contributing to continuous improvement initiatives.
  • Experience working independently, managing priorities, and delivering work across multiple activities or projects.
  • Proven performance in earlier role.

Moreover, you meet the following personal skills and competencies:

  • Strong attention to detail and data accuracy.
  • Excellent analytical and problem-solving skills.
  • Understanding of business processes within supply chain, procurement, quality and finance.
  • self-starter, initiative-taking.

The proposed gross annual/hourly 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 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).