Edward J Turgeon's Location
Lexington, South Carolina, United States, United States
Edward J Turgeon's Contact Details
Edward J Turgeon work email
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Edward J Turgeon personal email
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About Edward J Turgeon
Seasoned MS/BS chemical engineer with a business acumen provided from an MBA in management. Accomplished track record in project management, process engineering, technology transfer, and continuous improvement within a cGMP manufacturing environment. Diverse experience from working in all phases of a process life cycle: from conception and justification, through preliminary design, collaboration with R&D process development and technology transfer, oversight of detailed design, procurement, construction and commissioning, and directing system qualifications (IQ/OQ), systems start-up with process validation (PPQ), and commercial manufacturing with continuous improvement (CPV).. Certified Six Sigma Green Belt, experienced supervising all aspects of operations, where passion for continuous improvement had led to numerous gains in yields and productivities for several products.Strengths include sharp attention to detail, strong analytical reasoning skills, coupled with exceptional planning and organizational abilities. COMPETENCIES: Project Management, Process Design, Technology Transfer, Process Safety, Team Leadership, Continuous Improvement, Qualification & Validation
Edward J Turgeon's Current Company Details
Retired - Open to short term remote/hybrid special projects
Edward J Turgeon Work Experience Details
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Principal EngineerSanofi Genzyme Jan 2020 - Apr 2023Framingham, MaServe as corporate engineering consultant to Site Engineering at various Sanofi facilities for their project design development to assure compliance to Sanofi worldwide standards and practices are employed for technical deliverables during all stages of projects; feasibility studies, conceptual design, detailed design, and construction execution. . Provide support for technology transfers of drug substance for clinical/commercial manufacture at internal and external facilities. • Provided oversight for conceptual and detailed design of a manufacturing suite revamp to accommodate a new Cell Therapy product. Reviewed and approved development of project drawings, URS, CQV protocols, and SOP’s for related equipment and utility systems. • Provided oversight for conceptual and detailed design for New Product Introduction (NPI) to an existing manufacturing suite, performing reviews of all drawings, specifications, and vendor proposals. The project is currently successfully proceeding through various commissioning studies. -
Senior Process EngineerAlkermes, Inc. 2016 - Nov 2019Greater Boston AreaServe as manufacturing technical consultant to Alkermes Process Development for products in Phase III, while supporting all aspects of the manufacture of drug substance at third party manufacturers for established products. • Developed vendor selection guidance documents to proceduralize and standardize business practices, with vendor attribute scoring for three stages of selection; Candidate Identification, Secondary Screening, and Due Diligence. This includes compilation of a multi-functional questionnaire to use within an RFI or RFP.• Developed cost estimate models to compare two inventory risk mitigation approaches (higher reserve versus secondary supply) for either generic or proprietary drug substances.• Advocated adoption of Design Space approach to establishing process operating parameters and to assure bracketing of Normal Operation Range (NOR) between Proven Acceptable Range (PAR) for regulatory filings.
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Project Manager (Contract Position)Lonza Sep 2015 - Apr 2016Portsmouth, NhLonza lead for multi-disciplinary teams in completion of technical deliverables through all project phases, including feasibility, conceptual, clean room layout design, and detailed design for both cell therapy and mono-suite facilities. Coordinated and managed team activities to meet scope, schedule, budget, safety, and quality requirements for capital projects.
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Fermentation Lead Engineer, At Bp Biofuels Na LlcBp Feb 2011 - Mar 2015Houston, TxTeam Leader/resident engineer at CH2M Hill Houston engineering offices for the process design of propagation and fermentation areas for 10, 18, and 36 MMgal/yr scale Ligno-Cellulosic Ethanol facilities, for both green field and ‘bolt-on’ project scopes. Guided design development efforts of PFDs and P&IDs, crafted project & process engineering procedures, design guidelines, equipment and piping specifications in accordance with the planned project schedules.• Directed the design development of multiple-stage industrial propagation systems of fermentation organisms and saccharification enzymes, in addition to process units for ethanol fermentation, media preparation & sterilization, and design of CIP systems. • Performed value engineering assessments for processing alternatives (batch vs. fed-batch, continuous) and equipment modifications to reduce capital and operating costs. -
Principal Process Engineer, At Bp Biofuels Na LlcBp Aug 2010 - Feb 2011Naperville, IlManaged multiple concurrent projects involving front end engineering design, cost estimation, and project justification for incremental improvements to the Jennings Demonstration Scale Cellulosic Ethanol Facility. • Led a multi-functional team to investigate contaminations and identified several hygiene deficiencies in the original system design, construction, and operational procedures of fermentation area production units. Directed the implementation of corrective measures that resulted in significant reduction in contamination.• Co-editor and contributor to “BP Biofuels Plant Hygienic Design Guidelines” document that conveyed key concerns for the proper design of equipment & piping for use in hygienic processes and Clean In Place systems.
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Senior Manager - Process EngineeringVerenium Biofuels Mar 2008 - Aug 2010Cambridge, MaPrimary engineering liaison with both Operations and R&D; guided and coordinated activities of technology transfers to advance the development of fermentation process technology to improve processing capabilities, increase productivity and product yield, and to help reduce raw material costs. Guided trouble shooting efforts to correct problematic performance issues with industrial operations in both Pilot Scale and Demonstration Scale facilities. -
Technical ManagerPfizer Inc. Pgm 2004 - 2008Groton, CtAssessed scheduled product campaign process fits within available equipment to identify potential need for equipment/instrument modifications. Devised plans and supervised efforts for the implementation and qualification of needed modifications for product campaign startups to assure compliance with product delivery forecasts.• Plant Safety Committee Leader: Established team, recruited and coached membership, coordinated activities of team including; issue investigations, risk ranking, prioritization, development and tracking of resolution implementation for safety suggestion submissions to improve site-wide overall safety. -
Sr. Manufacturing EngineerPfizer Inc. Pgm 2000 - 2004Groton, CtSupervised operations to assure compliance with regulatory requirements on quality and yield while maintaining cost standards. Investigated out of trend and specification deviations to identify root causes with aid of QA/QC. Developed, implemented, and documented corrective actions and preventative measures.• Formed and led cross-functional Process Improvement Team for key products that identified, prioritized, and implemented equipment and operational modifications to improve product quality, yields, and reduce cycle times. Achievements included yield increases up to 2.5%, batch cycle reductions by 30%, improved product quality and operational consistency.• Recipient of a Pfizer Quality Award for leading a process improvement team with significant operational performance results of increased yields and improved productivities.
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Design ManagerPfizer Inc. Pgm 1998 - 2000Groton, CtPfizer resident Design Manager at Engineering firm for an $80MM process modernization project with Delta-V automation for a multi-product API organic synthesis facility, and then later for $20MM specialty product enabling project. Directed the multiple discipline detailed design effort, reviewed documents for accuracy and compliance to specifications, established metrics for engineering vendor bid analyses, tracked design/procurement deliverables progress for adherence to schedule and budget. Achieved construction-issue document qualities that resulted in field change rates at only one third of historical rates (i.e. 67% reduction in field changes). • Led design-build contract from conceptualization through qualification for custom chemical containment equipment for selected materials transfer operations, covering the charging and packaging of both liquids and solids to help limit operator chemical exposures.• Provided technical expertise to PHA safety reviews of process and utilities systems, prioritized and tracked completion of resultant action items, and supervised allocation of resources to address identified safety issues.• Supervised operator teams in performance of system commissioning; developed and supervised execution of IQ/OQ protocols for both processing and utility systems. Compiled, prioritized, and tracked completion of system deficiency “punch-list” items to assure completion for system qualification closeouts.
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Project Manager / Sr. Project EngineerPfizer, Us Pharmaceuticals 1994 - 1998Groton, CtManaged the FEED, capital justification, detailed design, procurement, installation, commissioning, and turn-over for multiple con-current (ROI, upgrade, environmental, and safety driven) projects with investments from $50K to $20MM, each within budget, on schedule, and meeting customer requirements.• Led multi-disciplined team that investigated site-wide steam condensate return systems to improve central utility boilers’ overall economics via increased condensate return fraction and achieved targeted reduction in visible steam plumes from building roofs. Lead author for the Pfizer divisional “Condensate Return System Design” ‘best practice’ document.• Authored “Piping Design for Clean-In-Place” design guide document for use within Pfizer based upon the learnings from a CIP feasibility study project with consultant Dale Seiberling.
Edward J Turgeon Skills
Process Engineering
Engineering
Continuous Improvement
Manufacturing
Process Simulation
Project Management
Technology Transfer
Validation
Cross Functional Team Leadership
Process Improvement
R&d
Gmp
Commissioning
Chemical Engineering
Analysis
Biotechnology
Contract Management
Procurement
Contract Negotiation
Energy
Team Leadership
Budgets
Process Safety
Six Sigma
Process Optimization
Project Planning
Quality Assurance
Automation
Start Ups
Product Development
Management
Fermentation
Lean Manufacturing
Renewable Energy
Ms Project
Budget Management
Cgmp
Research And Development
Business Process Improvement
Capa
Edward J Turgeon Education Details
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Management -
Chemical Engineering -
Chemical Engineering
Frequently Asked Questions about Edward J Turgeon
What is Edward J Turgeon's role at the current company?
Edward J Turgeon's current role is Retired - Open to short term remote/hybrid special projects.
What is Edward J Turgeon's email address?
Edward J Turgeon's email address is ed****@****mes.com
What schools did Edward J Turgeon attend?
Edward J Turgeon attended Bryant University, University Of Rhode Island, University Of Rhode Island.
What skills is Edward J Turgeon known for?
Edward J Turgeon has skills like Process Engineering, Engineering, Continuous Improvement, Manufacturing, Process Simulation, Project Management, Technology Transfer, Validation, Cross Functional Team Leadership, Process Improvement, R&d, Gmp.
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