The Associate Director Quality Control (QC) will lead QC activities associated with the GMP production. Such products include Adeno-associated Viral Vectors (AAV) and Retroviral Cell Therapy Vectors. This position will oversee the operation of the QC Microbiology and Transport functions. The Director is responsible for supporting the QC testing, utility and environmental monitoring and overall support for clinical and commercial product manufacturing. Responsibilities   + Implement and manage a GMP compliant laboratory control program in adherence to current FDA Guidelines, ICH, and foreign regulations in the areas of microbiology, methods, validation and stability + Planning and execution of QC testing to ensure agreed upon cycle times are met, associated records are evaluated and data are accurate, valid, and complete + Responsibility for ensuring completion of release testing of raw materials, process intermediates, packaging components, and drug products + Maintain and trend environmental monitoring and personnel monitoring programs to ensure compliance to regulatory requirements + Support CMO production activities by coordinating testing activities with appropriate external and in-house departments + Support in-house production by co-ordination of in-process QC testing, environmental monitoring, and release/characterization testing with appropriate departments/CTOs + Prepare specifications and Certificates of Analysis (COA) for QA review + Establish and execute stability programs for raw materials, cell and viral banks, drug substances and drug products + Coordinate with the Analytical Methods Development group the phase appropriate qualification/ validation of microbiology procedures, the transfer of such procedures into QC Microbiology, and the setting of appropriate acceptance criteria + Manage the development, validation, and approval of all microbiology, and raw materials test methods used in production operations as well as Assay Transfer with external customers or CMO/CTOs + Oversee QC activities at CMOs and CTOs, including the review and approval of test records/forms, final reports, Standard Operating Procedures (SOPs) and COAs + Draft and review of SOPs, records/forms and protocols for in-house QC testing and overall QC operations + Assist in the preparation of CMC regulatory submissions + Interact with the FDA and other worldwide regulatory agencies, per product filings (IND, BLA MAA etc.), regarding any questions relating to microbiology, stability testing and inspection of drug product + Conduct investigations into atypical and out-of-specification test results internally and externally + Other activities as may be assigned Requirements   + A minimum of Bachelor’s in Biological Sciences, Bioengineering or Chemistry + Minimum of 7 years of experience in the biotechnology or pharma industry with a primary focus on analytical QC for biologic products + Minimum of 3 years demonstrated track record of leadership and management of QC groups with people development and performance management skills + In-depth experience of QC analytical methods and regulatory/pharmacopeia requirements for biologic product testing and method validation + Experience managing CMO/CTO relationships preferred + Excellent interpersonal, organizational, and written/oral communication skills Powered by JazzHR