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Director, CMC Lead – ADC Portfolio (Europe)

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Director, CMC Lead – ADC Portfolio (Europe)

ppWuXi 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. /p h3About the job /h3 h3Summary /h3 pThe 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. /p pThis position will offer the candidate flexibility working remotely from home in Europe. /p h3Responsibilities /h3 ul liProvide project and portfolio leadership to support IND‑enabling and late‑stage CMC activities for bioproduct development. /li liPartner with cross‑functional CMC teams to ensure successful execution of ADC and bioconjugate CMC programs, delivering high‑quality results on time and within budget. /li liSupport development and manufacturing alliance management, as well as product development and manufacturing strategy. /li liCoordinate cross‑functional efforts and facilitate clear communication to ensure strong alignment between WuXi XDC and clients. /li liLead and collaborate with a high‑performance team to ensure delivery of best‑in‑class services. /li liStrengthen existing service offerings and contribute to business growth by developing new client opportunities. /li /ul h3Technical Skills / Knowledge /h3 pDemonstrated strength in project management, problem‑solving, and interpersonal communication, with a proven ability to work effectively across diverse technical, business, and operational functions. /p ul liSolid understanding of the pharmaceutical industry and end‑to‑end large‑molecule drug development. /li liTitle for this CMC Lead role is flexible, ranging from Associate Director and Director to Senior Director. /li liDepending on title level, 5–15 years of relevant experience in pharmaceutical or biotech CMC process development and/or GMP manufacturing is required. /li liStrong working knowledge of current regulations, quality expectations, and industry trends related to large‑molecule and ADC/bioconjugate development, manufacturing, and testing. /li liPrior hands‑on experience with ADC programs is preferred. /li liExperience working within a CRO or CMO environment is preferred but not required. /li /ul h3Education and Experience /h3 ul liPhD in biochemistry, molecular biology, biochemical engineering, pharmaceutical science or related discipline. /li liFluent in English and Mandarin Chinese. /li liMust have working knowledge of MS Office products. /li liTechnical experience at large pharma or biotech companies. /li liADC/Biologics process/formulation/analytical development and/or manufacturing experience /li /ul /p #J-18808-Ljbffr

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