Jose E. Torres-Serrano Email & Phone Number

Bedford, Massachusetts, United States

Cambridge, Massachusetts, United States

Cambridge, Massachusetts, United States

Responsible for the Quality Organization (Quality Assurance and Quality Control) overseeing the GMP operations at the CRISPR in-house manufacturing facility for the production of Cell Therapy and Gene Editing products.

South San Francisco, California, United States

Accountable for providing quality oversight for drug substance and drug product manufacturing activities including review of executed batch records, batch release and change control processes associated with manufacturing activities. Responsible of overseeing investigations associated to the drug substance/product manufacturing and analytical activities, constantly collaborating with cross-functional teams in their completion and resolution.

Bothell, Wa

Accountable for leading and managing day-to-day activities associated with the QA Operations department with the goal of meeting the site’s business objectives as the site increases its focus on commercial manufacturing and advancing development products through commercialization. Responsibilities include leading the following operations within QA: Lot Disposition, In-Plant QA, Raw Materials, and Supplier Quality Management. It also includes continuously interfacing with cross-functional teams, such as Manufacturing, Facilities, Quality Control, Supply Chain, and Project Management as well as other sites across the AGC Biologics’ network.

Japan

Acting Head of Quality accountable of leading the Quality Operations (QA and QC) at the AGC Biologics sites located at Chiba and Yokohama, Japan. Member of the Global Quality Leadership Team and Site Leadership Team. Responsibilities include Quality Systems, Quality Control, tech transfer activities, and expansion activities. It also include the support to the general operations at the sites, ensuring that all critical areas (i.e. Manufacturing, Supply Chain, etc.) are in continuous compliance state and inspection ready.

South San Francisco, California, United States

As part of the Commercial Quality Systems Team at Genentech, responsible to lead the Lot Disposition and Document Management Teams, addressing a diverse scope of complex problems and initiatives to meet cGMP regulations and Genentech standards. In addition, responsible to manage performance and development of direct reports to ensure achievement of organizational and department goals and a productive environment.

Thousand Oaks, Ca

Integral part of the Contract Manufacturing and Contract Small Molecule Quality cross-functional and multi-site leadership team that includes Operations, Process Development and Supply Chain.

Louisville, Kentucky Area

As part of the Corporate Manufacturing Performance Management (CMPM) team, responsible to manage local and global-scale projects towards successful completion.

Louisville, Kentucky Area

Responsible for the supervision of the Logistics staff and operations at the Amgen Louisville Distribution Center in the receiving, storing, dispensing, and transferring/shipping of materials/finished goods in compliance with all regulations, procedures and Quality guidelines.

Louisville, Kentucky Area

Juncos, Puerto Rico

Barceloneta, Puerto Rico

Masters Degree, Quality Management (Manufacturing Competitiveness)

Bachelor Of Science (B.S.), Biology

Biology, General