FUJIFILM

  • Director, Quality Assurance Compliance

    Job Locations US-TX-College Station
    Posted Date 6 months ago(5/7/2019 3:48 PM)
    Requisition ID
    2019-3894
    Category
    Quality Assurance
    Company (Portal Searching)
    FUJIFILM Diosynth Biotechnologies U.S.A., Inc.
  • Overview

     

    Summary:  The Director, QA Compliance will be responsible for oversight of QA Compliance for cGMP manufacturing of monoclonal antibodies and Gene Therapy/Viral products.

    The individual will work with global and site Quality to implement, maintain and improve Quality Management Systems and programs to maintain FDBT facilities inspection ready.

    External US

    Essential Functions:

     

    • Leadership
      • Mentor and provide direction to the QA Compliance organization to ensure organization is complying with site and global quality standards, regulatory requirements and partner commitments
      • Collaborate across the organization to implement global and site compliance standards to ensure facility inspection readiness
      • Work with Quality management on staffing of QA Compliance organization
    • Operational Delivery
      • Lead Partner and Agency GMP inspections and manages commitments to corrective actions
      • Direct internal and external audits and maintains audit schedule
      • Collaborate with site leadership and QA Operations to develop and maintain a risk based strategic Compliance plan for the FDBT facilities that will meet US and EU requirements for cGMP manufacturing of drug substance and sterile drug product
      • Support on time release of manufactured products
    • New Business Growth
      • Host due diligence Quality audits
    • Compliance
      • Negotiate Supplier Quality Agreements
      • Negotiate Partner Quality Agreements
      • Review and/or approve basic and complex technical documents, including but not limited to:

    Standard Operating Procedures

    Change Controls

    Deviation and Investigation reports

    Annual Product reports

    • Work with Quality management to implement and grow phase appropriate quality systems that will enable cGMP manufacturing of pre-clinical to commercial products
    • Provide daily guidance for the compliance of Facility with international standards and regulations for GMP manufacturing
    • Support Regulatory, client, and internal audits
    • Act as a QA liaison to internal Departments and external Client Quality Groups and Vendor/Contract Laboratory Quality Groups as requested
    • Promptly notify Senior Management of potential quality or regulatory issues that may affect site or global compliance

     

     

    Required Skills & Abilities:

     

    • Ability and desire to learn and undertake additional leadership responsibilities across all Quality Assurance functions
    • Excellent written and oral communication skills.
    • Excellent organizational, analytical, data review and report writing skills
    • Ability to set personal performance goals and provide input to departmental objective
    • Ability to multitask and easily prioritize your work
    • Ability to work independently with little supervision
    • Proficient in Microsoft Excel, Word and PowerPoint
    • All candidates must have a working knowledge of cGMP regulations for the production of drug, biologics or vaccine products

     

    Working Conditions & Physical Requirements:

    The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.  While performing the duties of this job, the employee is regularly required to:

    • Experience prolonged standing, some bending, stooping, and stretching
    • Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required
    • Attendance is mandatory

     

    Qualifications:

    BS or equivalent with 6+ years of Quality experience in a regulated pharmaceutical, biotechnology or supporting CMO environment.  Experience with electronic quality management systems.  Strong knowledge of US and European compliance requirements.  Strong knowledge of facility engineering and commissioning, biotechnology manufacturing, utility commissioning, regulatory approval process and requirements.  Direct experience hosting or supporting Regulatory agency site inspections.

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