CMC Regulatory Dossier Management Director

CMC Regulatory Dossier Mgmt Director page is loaded## CMC Regulatory Dossier Mgmt Director locations:
Alameda, CAtime type:
Full time posted on:
Posted Yesterday job requisition :
JR6488
** SUMMARY/JOB PURPOSE** **(Basic purpose of the job):
** This role provides PSC Regulatory expertise and leadership for biologics and Bioconjugates commercial and development projects. Responsible and accountable for leading development of high-quality, phase appropriate regulatory sections and delivering documents to regulatory operations on aligned timeline. Responsible for developing strategy and supporting materials to support PSC related health authority interactions. Manages submissions to US investigational new drug applications (IND), ex-US clinical trial applications, and Biologics License Applications (BLAs) and ex-US license applications.

This role works closely with the Bio CMC (Chemistry, Manufacturing and Controls (CMC)), Regulatory Affairs CMC and Quality Assurance departments, as well as with cross-functional project teams.
** ESSENTIAL DUTIES/RESPONSIBILITIES:
*** Lead development of high quality, phase appropriate CMC-related submissions to regulatory authorities and regulatory affairs. Tracks progress of authoring, reviewing, approving and submitting to publishing, including submissions across multiple countries and clinical studies.
* Lead development of responses to health authority questions and documentation requests.
* Ensure appropriate archiving of source technical documentation.
* Lead review of chemistry, manufacturing, and controls-related documentation (e.g., INDs, IMPDs, NDAs, BLAs) with SMEs, CDMOs and Exelixis leadership. May be required to provide relevant content or develop documents and templates as necessary.
* Track and manage external partner regulatory actions, documentation associated with regulatory actions in both post-approval and development stage changes through completion.
* Liaise internally with Regulatory Affairs CMC to coordinate CMC changes with other aspects of the development programs.
* Ensure continued regulatory compliance and phase appropriate, risk-based approaches to manufacturing flexibility while adhering to change control procedures and health authority requirements.
* Monitor Biologics CMC regulations and guidance to assess relevant changes and implications to current and future development and commercial activities.
* Contribute to the implementation of processes and procedures, including developing and authoring internal work instructions and company SOPs.
* Work with cross-functional teams to identify and support continuous improvement opportunities for processes and systems.
* Provide strategic and forward-looking guidance regarding processes and systems surrounding review committees.
* People management responsibility and oversight (through direct reports and as an individual contributor as needed) within Bio CMC and cross-functionally.
* Contribute to the optimization and implementation of processes and procedures, including developing and authoring internal work instructions and company SOPs and identifying solutions for process optimization and efficiency commensurate with departmental and company growth.
* Lead internal preparation of CMC strategy in support of any required meetings with Regulatory Agencies and/or RFIs (Request for Information) from health authorities, including preparation of supporting documentation, as necessary.
* Liaise internally with members of Exelixis’ functional departments.
* Liaise externally with vendors, partners, and joint development collaborators.
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* SUPERVISORY RESPONSIBILITIES:

*** Leads or manages the work of others by providing guidance to subordinates or teams.
** EDUCATION/EXPERIENCE/KNOWLEDGE &

SKILLS:

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* Education:

*** Bachelor’s degree in related discipline and a minimum of thirteen years of related experience; or,
* Master’s degree in related discipline and a minimum of eleven years of related experience; or,
* PhD degree in related discipline and a minimum of eight years of related experience; or,
* Equivalent combination of education and experience.
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* Experience:

*** Minimum sixteen years pharmaceutical industry and/or…