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BeiGene Associate Director, Technology Transfer in Emeryville, California

General Description:

BeiGene is seeking a highly motivated technical expert to join our small molecule drug product development organization in the U.S. The individual manages intercompany and intracompany technology transfer of late stage and commercial oral solid drug product. He/she will also provide technical support to the manufacturing of commercial drug products.

Level and compensation will be commensurate with experience.

Responsibilities:

  • Manage technology transfer projects and provide technical support to drug product technology transfer.

  • Collaborate with all relevant departments to complete technology transfer activities.

  • Coordinate internal and external resources to achieve the requirements of the project plan.

  • Facilitate/lead/coordinate technology transfers by assuring all relevant information and materials are successfully communicated and applied during manufacturing in accordance with agreed upon timeline. The work includes, but not limited to, reviewing/approving documents, transferring knowledge, providing process support, and preparing reports.

  • Track team activities and timelines to ensure that the deliverables are met timely.

  • Prepare, distribute, and present project status reports to project team members and management.

  • Manage and set priorities for specific projects/programs.

  • Provide project management and/or technical support pertaining to technology transfer.

  • Establish and maintain positive relationships with intracompany and intercompany (partners, CMOs) counterparts.

  • Manage, prioritize, delegate assignments and review work of direct reports.

  • Provide leadership to generate options to resolve problems, prioritize, and decide appropriate courses of actions, implement decisions.

  • Define, document, and establish controls for technology transfer and knowledge management, identify continuous improvement activities to improve performance.

  • Lead special projects as assigned.

Qualification:

  • PhD Pharmaceutical Science / Chemical engineering / Medicinal, Physical, Analytical Chemistry with 4+ years of industry experience, or MS with 6+ years, or BA with 8+ years of industry experience is required.

  • Experience in NCE product development and manufacturing science is highly preferred.

  • A deep understanding of pharmaceutical manufacturing processes is necessary along with ability to guide the generation and interpretation of formulation/process development data as it relates to the overall technology transfer.

  • Successfully demonstrated ability to manage and influence internal and external stakeholders and resources.

  • Prior supervisory experience is a plus.

  • Strong written and verbal communication skills.

  • Travel to manufacturing sites is required.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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