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Director, Cmc Lead – Adc Portfolio (Europe)

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Director, Cmc Lead – Adc Portfolio (Europe)

WuXi XDC (stock code: 2268.HK), a leading Contract Research, Development and Manufacturing Organization (CRDMO) focused on the global antibody drug conjugates (ADCs) and broader bioconjugate market, is a pioneering CRDMO offering integrated, end-to-end services. Services are provided from proximately located, state-of-the-art laboratories and manufacturing facilities, allowing for a significant reduction in development timelines and costs. Headquarter in Shanghai, China, our over 1,000 skilled employees work across a global network to deliver expert-driven, high-quality and right-first-time project execution for our customers. By offering a single-source, open-access platform with the most comprehensive capabilities and technologies, WuXi XDC enables our biopharmaceutical partners to speed the development of innovative therapies for the benefit of patients worldwide. About the job Summary The incumbent will lead the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical teams and business development team. The incumbent will also participate in business development activities such as visiting existing or new clients and promoting WuXi XDC’s services at conferences/trade shows. This position will offer the candidate flexibility working remotely from home in Europe. Responsibilities Provide project and portfolio leadership to support IND‑enabling and late‑stage CMC activities for bioproduct development. Partner with cross‑functional CMC teams to ensure successful execution of ADC and bioconjugate CMC programs, delivering high‑quality results on time and within budget. Support development and manufacturing alliance management, as well as product development and manufacturing strategy. Coordinate cross‑functional efforts and facilitate clear communication to ensure strong alignment between WuXi XDC and clients. Lead and collaborate with a high‑performance team to ensure delivery of best‑in‑class services. Strengthen existing service offerings and contribute to business growth by developing new client opportunities. Technical Skills / Knowledge Demonstrated strength in project management, problem‑solving, and interpersonal communication, with a proven ability to work effectively across diverse technical, business, and operational functions. Solid understanding of the pharmaceutical industry and end‑to‑end large‑molecule drug development. Title for this CMC Lead role is flexible, ranging from Associate Director and Director to Senior Director. Depending on title level, 5–15 years of relevant experience in pharmaceutical or biotech CMC process development and/or GMP manufacturing is required. Strong working knowledge of current regulations, quality expectations, and industry trends related to large‑molecule and ADC/bioconjugate development, manufacturing, and testing. Prior hands‑on experience with ADC programs is preferred. Experience working within a CRO or CMO environment is preferred but not required. Education and Experience PhD in biochemistry, molecular biology, biochemical engineering, pharmaceutical science or related discipline. Fluent in English and Mandarin Chinese. Must have working knowledge of MS Office products. Technical experience at large pharma or biotech companies. ADC/Biologics process/formulation/analytical development and/or manufacturing experience #J-18808-Ljbffr

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