Joseph Scott Email & Phone Number

La Verne, Ca, Us

Tustin, California, Us

- Continuing to build the Supply Chain organization to support the growing complexity and volumes of Avid's production operations.- Support the Operations leadership team and its growth in organizational management.

Foster City, Ca, Us

- Lead the Warehouse Ops organization to drive incoming material receipt, Manufacturing support and Finished Goods distribution- Coordinate 3PL Operations to support US Finished Goods Distribution- Project Management lead for cross-functional strategic inititatives (MES, EBS, Process Optimization, etc.)- Lead the Site Services Support Operations for both San Dimas and La Verne sites

Foster City, Ca, Us

- Lead the Project Management Office during the construction, commissioning, validation and site operational readiness for Gilead's new MFG facility in La Verne, California.- Manage Budget, Schedule, Scope and Communication to ensure project milestones are delivered on time and within budget.

Cambridge, Ma, Us

- Project Manager for the re-design, integration and implementation of a new shop floor scheduling process for our Biogen's Internal Manufacturing sites. Partnering with Infor to integrate different systems to deliver a comprehensive, real-time, visual schedule to improve schedule adherence and optimize communication.- Manufacturing Business Process Owner for a major overhaul and upgrade of our Oracle ERP system. Partnering with cross-site and cross-functional teams to ensure smooth transition of our upgrade and implementation of new modules onto the existing ERP architecture.

Cambridge, Ma, Us

• Managed >$170MM running inventory of the Hillerod Manufacturing site (Drug Substance and Drug Product)• Member of the Site Leadership Team driving critical initiatives towards site short/long-term goals (Safety, Quality, Deliver and Financial)• Led Commissioning/Validation and commercially-licensed GMP Manufacturing readiness projects at the 2000,000 SF international biopharmaceutical facility with 90,000L batch cell culture capacity.• Re-engineered standard business process and procedures to drive daily execution and enhance efficiencies across departments, specifically when introducing ERP modules and add-ons.• Managed the transition of the Warehouse and Materials Management operations in preparation for EMEA/FDA site approvals for commercial production.• Project Lead for Visual Work Instructions designed to improve the documents used by manufacturing associates to decrease errors and variability and increase productivity.

Cambridge, Ma, Us

• Managed and developed nine direct reports, focusing on effective cross-functional team leadership, project management and disciplined execution.• Transitioned the MFG Compliance group from deviation documentation into a team that takes complete ownership of RCA, Impact Assessment and effective Corrective Action identification/implementation.• Developed and implemented a standardized approach for compliance management, which drives a standardized/systematic approach to processing Trackwise events.• Led the Campaign Changeover Improvement initiative that significantly reduced the opportunity for error, enhanced compliance and improved efficiency. This includes the elimination of NVA activities (elastomer replacement, product specific assays and sampling requirements).• Led the Warehouse Optimization project using Lean Manufacturing techniques. Detailed process mapping of activities, followed by detailed SOPs created Standardized Work practices for enhanced compliance.• Sub-team lead for a Clinical vs. Commercial transformation project to evaluate more effective methods to manufacturing Clinical vs. Commercial products.

• CIP/SIP Validation of a new cell line being introduced to an existing facility.• Developed Qualification and Validation testing protocols for new Chemical R&D facility, including Receipt & Installation Validation, Functional and Performance Testing and IQ and OQ testing protocols.

• Led a team of eight Senior Technicians in order to complete directives on the manufacturing floor efficiently and successfully in a cGMP environment.• Involved in the transformation of existing procedures and policies to comply with lean manufacturing methods, including 5s, Kanban, Kaizen, “mistake-proofing” and six sigma DMAIC/DMADV.• Assisted with root cause analysis, CAPA, review, and approval of any necessary investigational reports to facilitate rapid closure of deviations and ensure actions are taken to prevent recurrence.• Participated in the creation/implementation of Area Core Skills Training program aimed at making the introduction of new technicians safe and effective in a cGMP environment.• Involved with Manufacturing Systems Improvement in developing and producing metrics data and tables for Manufacturing presentations and website.

Emeryville, California, Us

• Researched ideal fermentation environments for recombinant proteins used in the development of Chiron’s blood testing division. • Small scale shake flask experiments were performed to determine optimal growth conditions for recombinant proteins. Data was presented and technical reports were written for the validation of these filings.• Validation of processes and equipment were performed on a regular basis, as well as preventative maintenance on all fermentation and lab equipment

• Developed all operating procedures in a start-up Microbrewery, including all recipes, fermentation cycles, yeast management, and quality control.• Designed and built laboratory for quality control and testing of all products.• Developed bottling line for operations that meet ATF and health regulations and maximize efficiency and quality with the product.

Doctor Of Education - Edd, Organizational Leadership

Masters, Business Administration; Supply Chain Management

Bachelor Of Science, Cell And Molecular Biology

Fermentation Science Certificate Program