STEMSourcing

Senior/Executive Director Process Research and Development & Manufacturing

STEMSourcing California, United States
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Frances Todd

Frances Todd

Search Consultant at STEMSourcing

Our client, a thriving clinical stage biotech in California, is seeking a highly qualified and talented candidate for their team. Key functions of this exciting and fully remote role will involve:


  • Independently design synthetic routes to target molecules, conduct Process Research and Development, and manage API process research and development projects to develop cost-efficient, scalable and robust drug substance manufacturing processes.
  • Establish drug substance (including the related raw materials and intermediates) development manufacturing routes and strategies.
  • Provide strategic planning as well as technical support and oversee and manage contract manufacture organization (CDMO’s) to prepare manufacturing batches, development reports and other development-related documents.
  • Guide external third parties through technology transfer, process development, optimization, qualification and validation of the activities related to DS manufacturing operations. Be on-site, as necessary.
  • Collaborate with other functions to assure compliance with applicable GMP and global regulatory requirements.
  • Author and review of CMC sections for regulatory filings (INDs, IMPDs, NDAs, MAAs).
  • Provide technical strategic support and documentation for answering questions during regulatory submission reviews.
  • Supervise and manage CMC chemists and related staff.


They are looking for a candidate with:


  • Ph.D. in organic chemistry or related discipline.
  • A minimum of 12+ years’ industry experience in process research and development and CDMO management.
  • Strong knowledge cGMP requirements relating to drug substance.
  • Strong knowledge of drug substance process development and manufacture for early development. Knowledge of late development such as process registration, validation, and launch, a plus.
  • Excellent planning and organizational skills.
  • Able to make international and domestic travels.
  • Thorough understanding of cGMP compliance and ICH guidelines.
  • Experience with managing outsourced projects with contractors.
  • Strong leadership, teamwork, and collaboration skills.
  • Ability to thrive in a highly entrepreneurial, fast paced, and capital efficient environment.
  • Strong written and communication skills; and an ability to work effectively with a diverse team of co-workers in a dynamic environment.

  • Seniority level

    Executive
  • Employment type

    Full-time
  • Job function

    Manufacturing, Research, and Management
  • Industries

    Biotechnology Research and Pharmaceutical Manufacturing

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