Director/Executive Director of Cell Science
杭州奕安济世生物药业有限公司HangzhouUpdate time: May 14,2019
Job Description
Qualifications:
    Basic Qualifications:
  • Ph.D. in Biochemical Engineering, Cell Biology, Biochemistry, Bioengineering, or related fields and 5 plus years of relevant industry experience.
  • Experience working independently, manage teams, multitask, and to provide leadership.
  • Experience with the application of scientific and technical knowledge in contemporary bioreactor-scale mammalian bioprocess development and process optimization.
  • Experience with mammalian bioreactor systems 500L working volume.
  • Experience with chemically-defined mammalian cell culture media/feed design and optimization.
  • Experience with perfusion mammalian cell culture processes
  • Team player, experience working collaboratively and productively with interdisciplinary teams/functions, downstream counterparts, and external vendors to meet objectives.
  • Experience with Design of Experiments (DOE) approach for process development and characterization desirable.
  • Experience with formal technology transfer from pilot plant to commercial production
  • Experience with China and/or US/EMEA IND/BLA filing

  • Preferred Qualifications:
  • It is desirable to have a solid understanding of current Good Manufacturing Practices (cGMPs) requirements and considerations.
  • Must work well within a fast-paced, dynamic and team-oriented environment.
  • The candidate should be self-motivated, strongly driven to succeed, inquisitive, and have excellent organizational, interpersonal, communication and problem-solving skills.
  • Capable of directing cell line development.
    Responsibilities:
  • The Process and Product Development within HJB is to develop novel and biosimilar protein drugs and processes for phase I to commercial manufacturing. We also take in charge of development and implementation of products and processes developed by our US partners for China regulatory filing. This department is responsible for the development and implementation of “state of the art” and innovative technologies required to demonstrate and mature the production platform for therapeutics. This group will support implementation for clinical and commercial manufacturing in Hangzhou‘s “State of art” facility. This is an exciting opportunity with the potential to have a significant impact on future biologics manufacturing technology.
  • We are seeking a Director/Executive Director with extensive experience in mammalian cell culture process development. The successful candidate will be expected to work collaboratively with our US partner and drive the technology transfer and development of highly intensified, state-of-the-art, chemically-defined and highly productive upstream processes, and to integrate such processes with downstream development to ensure a robust, well-controlled, and well-understood biopharmaceutical manufacturing platform.
  • This person needs to be a highly motivated, organized, flexible and creative individual. He/she is a problem solver, willing to take calculated risks if necessary to achieve the desired goals, must be able to set team goals and define strategies to achieve them, and to provide leadership within a critical function. This person must be able to establish good working relationships with our US partners, vendors and internal colleagues (e.g. engineering, downstream, analytical) key to the establishment of a fully integrated platform, and to effectively represent these activities and the platform to senior management and across a global organization. This position is required to support technology transfer into cGMP/commercial biomanufacturing facilities. This is an exciting opportunity to participate in new technologies development and implementation into real world applications.
  • The head of upstream process development will develop models for resource, economic, and/or process analysis, in charge of group budget.

If you are interested
please submit your resume to: hr@transcenta.com

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