Tony Moorcroft Email & Phone Number

Thailand

Bangkok, Bangkok, Th

Company owner and principal consultant

Omaha, Us

Tokyo, Jp

Us

Contracted to Forest Pharmaceuticals OH as the C&Q Lead for the Kenwood road facility CINergize project – new construction of a solid dosage/liquids packaging facility comprising primary/secondary packaging suites, support areas and warehousing.• GMP regulatory C&Q planning and scheduling of deliverables• Delivery of facility system DQ protocols/reports and C&Q protocols/reports through room environmental and utility PQ• Turnover documentation content review• Progress monitoring and reporting to project leadership

Paris, France, Fr

Contracted to Genzyme MA as the C&Q Lead for the Allston Landing Facility Suite 2 Cerezyme Conversion Project – refurbishment under Consent Decree of bioreactor upstream and purification downstream process, utility and room systems. • C&Q planning and scheduling of deliverables• Resource identification, hiring and purchase requisition administration• Delivery of system impact assessments and C&Q protocols/reports through steam in place and room environmental PQ• Consent Decree audit team Liaison and escalation lead for Suite 2 associated capital projects• Execution of commissioning and qualification field activities, troubleshooting and nonconformance resolution• Documentation deliverable and field execution progress monitoring and reporting• Engineering Turnover Package administration

Paris, France, Fr

(Swiftwater site PA) contracted as the C&Q Execution Lead for the B37 Retrofit Project – refurbishment of the manufacturing wing of the Webster building comprising new and existing equipment• Developed and implemented execution strategies aligned with the Project C&Q Plan and SOPs• Providing C&Q timelines and sequence inputs to the project schedule• Defined and sourced resources required to execute C&Q project activities• Developed and executed commissioning and qualification protocols• Progress monitoring and reporting to project/site leadership• Administrator of facility equipment decommissioning and recommissioning scope• Administrator of area/system transfer of care custody and control(Acambis site MA) contracted to provide commissioning & qualification services for various projects.

San Diego, Ca, Us

Assigned to Ohio USA to provide construction and commissioning team management of capital projects including bulk manufacturing, packaging and pilot plant suites together with warehousing and office accommodation.Management oversight of capital project construction and commissioning teams.Liaison officer assuring seamless coordination between Site Operations and the project delivery teamCoordination of care custody and control transfer of areas and systems to OperationsAdministrator of client work requests and change managementDeveloper of educational tools, practices, procedures and templates to improve capital project delivery efficiency and cross departmental alliances.

Thousand Oaks, Ca, Us

Assigned to Puerto Rico to cross functionally support, guide and assist all capital projects implementing Amgen’s integrated Commissioning & Qualification (C&Q) program.Promote an integrated project delivery culture and guide to site groups on meeting the expectations of the C&Q program.Improve established site/project execution strategies by enhancing existing cross functional work streams.Feed the C&Q Core Team with new principles and concepts realized out of project execution, needs of project teams and industry trends.Assist Project Teams to report C&Q Progress.Continually improve the Amgen corporate C&Q program policies, practices and procedures.

Thousand Oaks, Ca, Us

Assigned to Rhode Island USA to manage the renovation of laboratory and manufacturing suites together with the construction of a new process development building.Coordination and management of the design/construction teams, vendors and specialist service provider.Management of the construction quality documentation, commissioning execution and turnover strategies.Provider of technical support into to Quality and Validation departments.Member of Amgen’s corporate Commissioning and Qualification Core Team tasked with providing the company C&Q strategy and program tools - Program outputs include:-• Integrated Commissioning & Qualification Operational Standard• Integrated Commissioning & Qualification Program Process Map• Integrated Commissioning & Qualification Training Narrated Slide Decks• User Requirement Specification Procedure• System and Component Impact Assessment Procedure• Design Qualification Procedure• Engineering Change Management Procedure• Quality Vendor Audit Best Practice• Construction Quality Plan Best Practice• Equipment Acceptance Testing Best Practice• Equipment Inspection Planning Best Practice• Calibration Planning Best Practice• Enhanced Turnover Package Best Practice

Rahway, New Jersey, Us

Assigned to Singapore to support the design, construction, commissioning and qualification of Merck’s pharmaceutical facility in Singapore.Commissioning and qualification strategic planning, rollout and alignment of project procedures and templates to meet Quality Unit GMP/GDP expectation.Management oversight of construction QC, commissioning and qualification teams.Review of executed IQ/OQ Protocols ensuring compliance with procedures and the assisting in the technical closure of discrepancies not requiring re-tests.Liaison officer between the Quality Assurance Department and Construction Team providing technical interpretation in both directionsPreparation of Purified Water OQ Protocol and Room Environmental PQ Protocols.Management of preventative maintenance engineering data acquisition and electronic entry into end user Maximo preventative maintenance system.

Dallas, Tx, Us

Lead Validation Engineer responsible for process equipment/utilities IQ/OQ for Merck Sharp and Dohme’s Pavia Project II Manufacturing Facility in Italy.Senior Validation Engineer responsible for the validation of Centocor’s Biotechnology Pharmaceutical Plant in the Netherlands. Responsibilities also included the design of the new facility HVAC Systems and on site technical expertise to resolve HVAC commissioning issues.

Validation Engineer, Lead Mechanical Design Engineer, and site based Project Engineer for Pfizer’s Pharmaceutical Sciences Building 510 in Sandwich UK.Lead Mechanical Design Engineer for the design of S.A.I.P.H’s Pharmaceutical Production Facility Tunisia.Lead Mechanical Design Engineer and site based Project Engineer for Laporte Industries, Wallis Laboratories, England.Lead Mechanical Design Engineer and site based Project Engineer for a Clean / Aseptic processing suite for Cyanamid Iberica in Madrid Spain.Lead Mechanical Design Engineer for the design of a set of tropical environment suites for ICI, England.Lead Mechanical Engineer assisting in the design of a clean / aseptic processing suite for Cyanamid UK.Lead Mechanical Engineer designing front-end HVAC concept schematics for a local consultant to develop together with the detailed design of a purified water and water for injection system for a set of clean room suites for Kahira Pharmaceuticals, Egypt.

Mechanical Design Engineer for the front-end design and cost engineering for a pharmaceutical production facility for Apothekernes Laboratorium, Norway.Mechanical Design Engineer assisting in the design of a solids production facility for C.P. Pharmaceuticals, England.Mechanical Design Engineer and site based Project Engineer responsible for the relocation and installation of secondary pharmaceutical process equipment and HVAC plant from Welling Garden City to Crawly for SmithKline Beecham.

Bachelor'S Degree, Environmental Engineering

General Engineering

General Engineering