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Manager, US Warehouse and Logistics - Princeton, United States - Genmab A/S
Description
At Genmab, we're committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.
The Role & Department
Reporting to the Senior Director, Supply Chain, US Warehouse and Logistics, the Manager, US Warehouse and Logistics will oversee the 3PL warehouse operation and supports Genmab's Qualification and Validation activities.
This role works with Quality Assurance to maintain GXP compliance throughout the warehouse and distribution network. This includes quality events handling - support investigations of quality events, external notifications and complaints, determine root causes, implement CAPAs, and drive closure. Contribute to FDA Reporting and Inspections. Support the maintenance and operations of Genmab key supply chain systems such as ERP and serialization.
Key responsibilities include:
•Oversee warehouse operation and distribution at 3PL and perform necessary Inventory management activities related to returns/destructions/recalls, change controls, deviations, CAPA's, external notifications and complaints - see below. Work closely with 3PL to influence, advise, and coordinate operational efforts across their warehouse operation.
•Lead the GXP vendor management compliance activities. Vendor onboarding, vendor evaluation, and GXP operational meetings with vendor.
•Support shipping validation and qualification of new packaging materials at 3PL.
•Support the maintenance and operations of Genmab key systems such as ERP (SAP) - as well as integration with 3PL and Serialization (Tracelink). If needed, support implementation of enhancement testing and validations.
•Work with Quality Assurance to maintain GXP compliance throughout the warehouse and distribution network. This includes quality events handling - support investigations of quality events, external notifications and complaints, determine root causes, implement CAPAs, and drive closure. Manage and maintain GXP documentation, data and procedures in Document Management system. Manage Recalls according to Genmab procedure. Prepare data for Quality Management Reporting and Annual Product Quality Review.
Requirements - what you must have
•Technical or technically oriented degree level, e.g. within engineering, technical operations, logistics or supply chain management.
•Minimum of 5+ years of working experience including experience with process and shipping validation for temperature-sensitive products.
•Experience within a global and controlled environment.
•Ability to travel overnights for business, estimated at 1-2 times per calendar quarter, total of 4-8 times per year.
Where you will work
This role will report to the Princeton, NJ office, and is hybrid.
For US based candidates, the proposed salary band for this position is as follows:
$91,875.00$153,125.00
The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as bonuses.
About You
Genmab leverages the effectiveness of an agile working environment, when possible, for the betterment of employee work-life balance. Our offices are designed as open, community-based spaces that work to connect employees while being immersed in our state-of-the-art laboratories. Whether you're in one of our collaboratively designed 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 guiding its unstoppable team to strive towards improving the lives of patients through innovative and differentiated antibody therapeutics. For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates. To help develop and deliver novel antibody therapies to patients, Genmab has formed 20+ strategic partnerships with biotechnology and pharmaceutical companies. By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSOTM) antibody medicines.
Established in 1999, Genmab is headquartered in Copenhagen, Denmark with locations in Utrecht, the Netherlands, Princeton, New Jersey, U.S. and Tokyo, Japan.
Our commitment to diversity, equity, and inclusion
We are committed to fostering workplace diversity at all levels of the company and we believe it is essential for our continued success. No applicant shall be discriminated against or treated unfairly because of their race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, or genetic information. Learn more about our commitments on our website.
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
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.