Daniel Adcock Email & Phone Number

Mishawaka, Indiana, United States

• Senior Leadership Team Member for a manufacturing site of 270 employees and $87 million budget• Personnel management for identification of resource needs, hiring, and performance evaluation• Director of Performance and Productivity System - identified and implemented initiatives across site and departments to achieve 5% organic savings (~$3 million)• Director of Project Management office - guided and coached a team of project managers for multisite and local level projects to set priority for return on investment and business need• Director of SAP ERP data system as acting administrator for the division including master data governance (MM), production planning (PP), quality (QA/QM), and finance (FICO) modules, including responsibility for training employees and data error troubleshooting.• Designed and authored appropriate master data change documentation to create consistency for all master data setup and change• Directed the communication and project plans between external suppliers for capital investment projects and material purchasing requirements totaling over $10 million

Mishawaka, Indiana, United States

• Established plans for new product introduction projects including architecture, construction, design transfer, validation, and commercialization of highly complex medical devices utilizing fully automated assembly equipment• Directed the new product introduction team of process, mechanical, electrical, and controls engineers to document requirements for installation of equipment and product launch• Established framework for process engineers to implement operator documentation and training requirements• Established framework for electrical, mechanical, and controls engineers to implement proper input and output requirements to meet validated process parameters• Created SAP implementation plans for new product introduction• Established SIOP meetings for new products to determine initial forecast and demand needs during commercialization phase• Transferred SIOP process to product health teams when commercialization phase was complete• Maintained production schedules during commercialization for manufacturing facility• Transferred production scheduling to production manager when commercialization phase was complete• Coached and developed team members for career advancement and performance evaluations

Elkhart, Indiana, United States

• Directed design transfer project managers for introduction of new processes and products• Coordinated production scheduling for 70+ processes and 15+ operators• Met with customers to obtain forecast and demand planning requirements for production planning in SAP• Met with suppliers on defined schedule according to supplier category and volume to create demand plan and receipt dates• Developed integration plans for SAP implementation for new processes and products• Maintained purchasing data in SAP for costing and reporting• Developed SAP change control process for design changes, process changes, and new processes and products• Directed teams design change projects for current processes• Directed teams for verification and validation activities for design changes and new products• Directed investigations for customer complaints for manufacturing/production related issues• Directed CAPA teams to identify root causes and implement solutions• Directed SCAR activities for raw material quality issues• Reviewed statistical data analysis for verification and validation requirements

Elkhart, Indiana, United States

• Directed design transfer teams for new processes, intermediates, and finished products• Established manufacturing controls for new processes• Authored process documentation according to the validated process for manufacturing personnel• Trained manufacturing personnel on documentation for new processes and products being transferred from R&D• Directed a team of process engineers to increase scale of new and current processes to support global demand• Evaluated non-conformances according to regulations and provided evidence to support CAPA/SCAR and usage decisions• Initiated production orders in SAP for production operators• Evaluated batch documentation for batch history file requirements• Evaluated in-process control non-conformances to determine usage decision• Developed complex chemical synthesis processes for global assay development• Executed statistical data analysis for design change evaluations, verification and validation, and new products

Tarrytown, New York, United States

• Established chemistry controls for raw materials, intermediates, and finished products• Evaluated raw material changes with chemical analysis to verify/establish equivalency• Authored design control documentation for evidence in design history files• Utilized analytical chemistry techniques to establish controls for intermediates and finished products (GC/MS, MALDI-ToF, HPLC, DLS sizing, ICP analysis, Zetasizing, electrophoresis)• Directed investigations of customer complaints or internal issues utilizing analytical chemistry methods to determine root cause• Evaluated new equipment needs and author business cases for capital investment• Established chemical conjugation group in the analytical chemistry lab department• Assisted accounts receivable and payable with SAP invoicing errors

Tarrytown, New York

• Launched research and development chemistry lab for global assay development site• Used statistical analysis software to determine optimized parameters for chemical processes• Used chromatography processes to purify raw materials and finished product• Created appropriate test methods to fulfill design control requirements for adherence to regulatory requirements• Authored design history and control documentation to adhere to regulatory requirements• Authored and create process procedures for chemical processes for use in manufacturing environments• Collaborated on cross functional NPD teams to determine design input requirement feasibilty• Executed experiments for determining optimal levels of chemical modification to meet quality and acceptance criteria requirements• Organized data and outcomes into SAP for design history requirements for regulatory compliance• Coordinated with audit response teams for regulatory audits by presenting and defending design history and design control evidence • Initiated purchase requisitions for R&D material including samples for evaluation• Developed presentations to executive level for required monthly peer review meetings• Characterized raw materials for control system creation• Executed test method characterization and validation for in process and final acceptance test methods

Master Of Business Administration - Mba, Healthcare

Bachelor'S Degree, Chemistry