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Who We Are At JD.com, also known as JINGDONG, we are building one of the world’s most trusted technology and supply chain ecosystems. What started as a bold idea in China has evolved into a NASDAQ-listed, Fortune 44 global enterprise serving over 700 million active customers. Powered by advanced logistics, innovative technology, and a commitment to integrity, JD.com operates across retail, logistics, technology, property and more, creating solutions that make everyday life smarter, faster, and more connected. Our Global Reach JD.com is expanding its international footprint through a digitally intelligent, cross-border supply chain and world-class logistics network, supported by platforms such as Joybuy, which brings trusted products to customers worldwide. Today, our teams operate across China, the U.S., U.K., Netherlands, France, Germany, Spain, Brazil, Hungary, Japan, South Korea, Australia, Thailand, Vietnam, Malaysia, Indonesia, Saudi Arabia, the UAE and beyond, reaching customers in every corner of the world. Learn more about who we are and what we do: https://corporate.jd.com/ About The Team You’ll be joining the JD.com team, which values collaboration, ownership, and a commitment to delivering high-quality results in a fast-paced, dynamic environment. What Youll Do 1.Last Mile capacity planning: Creation of structured capacity plans on a 1-6 months time frame 2.Last Mile Risk Mitigation: Monitor actual capacity to identify capacity risks and propose risk mitigation approaches 3.Execution analysis: Analyze and understand gaps between plan and execution and work with relevant stakeholders to rectify gaps 4.System and Process Optimization: Implement continuous improvement processes to constantly improve the quality of our last mile capacity 5.Peak Planning: Create and coordinate the execution of peak capacity plans About You 1.Education: Bachelors degree or higher; 1. Experience in capacity planning, capacity controlling 3.Proficient in Office software and solid data analysis and management skills. 4.Possess a strong sense of responsibility, strong communication and coordination skills, and strong logical thinking and problem-solving abilities. What We Offer Joining JD.com means becoming part of a company where people, innovation, and impact go hand in hand. We offer a competitive salary, a great location, and a supportive, people-first culture where your growth truly matters. With access to global projects, learning opportunities, and an inclusive environment that values every voice, you’ll have the space to shape the future with us. At JD.com, we’re committed to building a diverse and inclusive workplace where everyone can thrive. We’re proud to be an equal opportunity employer and make all employment decisions without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, disability, age, veteran status, or any other protected characteristic. Ready to apply? Take the next step in your career, apply now and explore the opportunities we have to offer.

Want to know more? ¿Es usted el solicitante adecuado para esta oportunidad? Descúbralo leyendo el resumen del puesto a continuación. At Algenex, we are passionate about advancing biotechnology through the development and manufacturing of recombinant proteins for the formulation of biological medicines. We are currently looking for an Analytical Development Scientist to join our team in Tres Cantos, Madrid. This is a great opportunity for a scientific professional who wants to play an active role in analytical development within a growing and innovative environment, contributing to projects with real impact on the future of biologic products. If you enjoy combining scientific rigor, technical problem-solving, cross-functional collaboration, and high-quality analytical work in a regulated environment, this role could be your next challenge. What are we looking for? We are looking for a proactive, detail-oriented, and scientifically driven professional with experience in analytical development, analytical validation, or quality control within the biopharmaceutical or biotechnology industry. In this role, you will contribute to the development, qualification, and validation of analytical methods, support product development across different stages, and help ensure robust, reliable, and compliant analytical data. The challenge! • Execute and coordinate analytical development, qualification, and validation activities of medium to high complexity., • Support different stages of Analytical Development and/or Analytical Validation with a high level of autonomy., • Design, follow, review, and improve analytical protocols, methods, and departmental procedures., • Analyze and interpret scientific data, ensuring technical consistency and reliability of results., • Document activities and results accurately and on time in accordance with cGxP, regulatory expectations, and internal procedures., • Plan, execute, analyze, and document stability, characterization, and validation studies., • Draft and review technical documentation such as SOPs, analytical methods, validation protocols, stability plans, and technical reports., • Design and execute analytical assays to support product development activities, including process development, formulation, characterization, and comparability, when applicable., • Develop, qualify, and validate analytical methods, including experimental planning, execution, data analysis, acceptance criteria definition, conclusions, and recommendations., • Generate and execute validation and stability protocols/plans and associated reports, including sample point tracking, trending, and result assessment., • Ensure timely and accurate recording of results and observations, maintaining data integrity and right-first-time documentation., • Review, consolidate, and approve documentation and results generated from your own activities and, when applicable, perform technical peer review of other team members’ documentation., • Ensure complete and consistent records, traceability, and compliance with ALCOA+ principles., • Identify technical issues and propose corrective and preventive actions., • Ensure the appropriate use and status of assigned analytical equipment., • Contribute to laboratory investigations, including OOS, OOT, and deviations, when applicable., • Participate in internal and external analytical transfers., • Keep electronic notebooks, raw data, logbooks, and related documentation up to date., • Support onboarding and technical training of new team members., • Collaborate effectively with peers, supervisors, and management to communicate progress, risks, and potential deviations., • Provide support to other company areas based on business priorities and operational needs. What do you need? • PhD, MS, BS, or Higher Vocational Training in Clinical and Biomedical Laboratory, or other disciplines related to Life Sciences., • Minimum 3–5 years of relevant experience in the biopharmaceutical or biotechnology industry in analytical development, analytical validation, or quality control., • Strong knowledge and hands-on experience in the development, qualification, and validation of analytical methods for biological products., • Practical experience working with biological samples and analytical techniques, including:, • HPLC: SEC, IEX, Reverse Phase, and Normal Phase, • ELISA: direct, indirect, sandwich, and inhibition, • cIEF, • CE-SDS, • Western Blot, • SDS-PAGE, • qPCR, • UV/Vis, • Other relevant analytical techniques, • Experience working in regulated environments and handling technical documentation accordingly., • Strong scientific data analysis and interpretation skills., • Professional level of English., • Experience with cGxP, ALCOA+, and management of OOS/OOT/deviations will be highly valued., • Flexible start time from Monday to Friday (full-time), • Benefits and Savings Club, • Training and language learning platform, • Wellness platform with unlimited free psychologist sessions, • Development plans and internal mobility policy What will the selection process look like? • Initial contact by phone, • 2 interview stages, • Final feedback at the end of the process Do you think this role is not for you? Stay connected with Algenex and follow our upcoming opportunities. The right next step in your career might be just around the corner. xqbhyrx EQUAL OPPORTUNITY COMMITMENT At Algenex, we are committed to equal opportunities and to fostering a diverse, inclusive, and respectful workplace. All applications will be considered without discrimination based on gender, gender identity or expression, ethnicity, nationality, religion, sexual orientation, age, disability, or any other characteristic protected by applicable law. #J-18808-Ljbffr

Compensaciones / Beneficios • Collaborate with product stakeholders to translate business needs into technical specs and timelines • Develop and customize features within the Stibo STEP platform (workflows, rules, WebUI, data models) • Write clean, documented code and participate in code revie