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@serestherapeutics.com
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Derek Floyd is listed as Senior Manager | Pharmaceutical | Bio-Pharmaceutical | Production Scheduling | Continuous Process Improvement | Supply Chain| Project Management | Planning | Production Operations | Performance Metrics KPIs at Self-employed, based in Aliso Viejo, California, United States. AeroLeads shows a work email signal at serestherapeutics.com, phone signal with area code 425, and a matched LinkedIn profile for Derek Floyd.
Derek Floyd previously worked as Pharma Manufacturing Operations Consulting at Self-Employed and Senior Manager, SC Pack Artwork, Performance & Processes at Seres Therapeutics. Derek Floyd holds Bachelor Of Business Administration (Bba), Minor - Information Systems from Cleveland State University.
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"The greatest achievements attained are completed in those acts of serving, helping, or inspiring others." Derek Floyd has more than 10+ very successful and rewarding years in the production planning and supply chain arena in the Pharmaceutical Industry. He is experienced in FDA, cGMP, and EMEA.His career really began when he joined Boehringer Ingelheim as a product inspector. Since then he has held positions ranging from Production Scheduler to Senior Manager Production Scheduling with the more recent role of Senior Manager SC Pack Artwork Performance & Processes. Derek takes great pride in working throughout his career with companies that have leading edge technologies that are saving lives and giving people a better quality of life. Derek really enjoys working in these environments and is very good at what he does. Indicative of Derek’s contributions, he has:•Acquired knowledge of Pharmaceutical and Biopharmaceutical manufacturing and processing including Sterile Parenteral Manufacturing, Immunotherapy cell production, Manufacturing of Clinical and Commercial Monoclonal Antibodies, Recombinant Proteins and Enzymes, Manufacturing of Peptides and Oligonucleotides, and Production of Microbiome Therapeutics.•Successfully solved discrepancies with the master schedule by communicating schedule changes to operators, and the Quality and Plant Operations team thereby maintaining a 0% schedule conflict.• Implemented efficiency programs resulting in average yearly savings of 450k (blue dollars), 3200 machine hours and 12,500 cumulative employee hours.Throughout his career, Derek has developed a reputation of being a very quick study, learning system methodologies as well as corrective and preventative action processes. He is known as a team player, working with cross functional teams, corporate, inter-corporate and multi-tiered management. Providing Consistency, Embracing Quality, Progressing with Purpose, Inspiring Excellence.Skills & ExperiencePharmaceutical/Biopharmaceutical Production: Parenteral | Immunotherapy Cell | Peptides and Oligonucleotides | Monoclonal Antibodies, Recombinant Proteins and Enzymes | Microbiome Therapeutics. Planning | Supply Chain | Business Process Excellence | Scheduling | Reporting | Analysis | Trouble Shooting Manufacturing | Quality System Methodologies | Operations | Analysis | Process Mapping | Metrics | Project Management | Leadership | MS Project | MRP | ERP | QAD MFG-Pro | Oracle | SAP | APICS Certification In-ProcessContact Information: Email: Derek.M.Floyd@gmail.comPhone: (657) 229-3323
Listed skills include Customer Service, Scheduling, Production, Pharmaceuticals, and 26 others.
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Consultant specializing in Master Scheduling, Supply Chain, Business Processes, and Business Process Excellence within the Injectable/Biopharmaceutical Clinical and Commercial manufacturing industry.
Cambridge, Massachusetts, Us
New role one month prior to company departure from mass layoffs – Reported to Senior Director Supply Chain, Global Product Demand Supply & Logistics. Responsibilities included: Developing end to end supply chain performance management programs across Global Logistics, Global Planning, Supply and Demand Management, Materials Management, Procurement, Regulatory, and External Supply, Commercial Readiness streams, and Product Delivery inclusive of the Quality Control teams for release testing completion and Quality Release teams for product release.
Cambridge, Massachusetts, Us
Reported to the Director, Clinical Manufacturing Operations. Responsible for ensuring efficient production of microbiome therapeutics through establishment of clear and accurate internal communication across departments, including clinical manufacturing, supply chain, GMP facilities and Engineering, quality control and quality assurance. Maintained integrated production schedule across internal and external manufacturing sites to support on-going and upcoming clinical trials. • Ensured cross-functional imperatives of Production planning with robust inventory planning for Commercial demand and Clinical supply manufacturing commitments • Established communication tools tailored to facilitate efficient production schedule discussions from routine meetings to leadership strategy sessions. Ensured daily production requirements were achieved to facilitate on-time delivery of commercial and clinical demand.• Provided project management support for critical process improvement and tech transfers activities and integrated key activities into the production schedule.• Created detailed site capacity tool for forward planning, capability and scenario planning.Seres Therapeutics is a commercial biotechnology company with a strong development pipeline and rigorous scientific underpinning, working to revolutionize treatment of a wide range of diseases by modulating the function of the human microbiome.www.serestherapeutics.com
Bubendorf, Ch
Production Scheduler (Life Science / Drug Development)Responsible for scheduling plant manufacturing resources. Work effectively with multiple departments to meet timelines. Serve as the primary user of the enterprise resource planning system (ERP). Work with the Production Manager(s) to create and maintain bills of material. Work with the production planning team in Switzerland to request new, final and intermediate products. Issue and update manufacturing orders as needed. Provide Production, QA, QC and Materials Management with required manufacturing order within required timelines. Work with Materials Management to update bills of materials to improve forecasting accuracyBachem Americas is an independent, technology-based, public biochemicals company providing full service to the pharma and biotech industry. Bachem is specialized in the process development and the manufacturing of peptides and complex organic molecules as active pharmaceutical ingredients (APIs), as well as innovative biochemicals for research purposes. With headquarters in Bubendorf, Switzerland, and affiliates in Europe and the US, Bachem works on a global scale and holds a leading position in the field of peptides. Specialties: Contract Manufacturing for Peptide Active Pharmaceutical Ingredients. www.bachem.com
Plan, schedule, coordinate and/or perform final approval of products through the production cycle. This role coordinates production plans to ensure materials are provided according to schedules to maintain production and provides input to management. Key functions include interfacing with project management, production, quality control and quality assurance to review back order status as well as prioritizing production orders and other potential schedule interruptions or rescheduling. The Master Scheduler/Planner works to resolve (in case of design changes) labor and material shortages. The position may oversee the master schedules and ensures comprehensive compliance with materials requirements for manufacturing.
Seal Beach , Ca, Us
Responsible for scheduling and monitoring activities related to logistics and manufacturing in support of the commercial and clinical manufacturing process. Facilitated and trained for effective working relationships with internal and external customers to ensure schedules are maintained within process and logistical constraints.• Developed and maintained final product schedule during increased business and maintained 100 percent scheduling success rate.• Successfully solved discrepancies with the master schedule by communicating schedule changes to operators, and the Quality and Plant Operations team thereby maintaining a 0% schedule conflict.• Used professional concepts in accordance with company objectives to solve complex problems in creative and effective ways.• Created KPI metrics for risk mitigation and operations management.Skills & Experience Pharmaceutical Parenteral Production | Biopharmaceutical Immunotherapy Production | Planning Supply Chain | Business Process Excellence | Scheduling | Reporting | Analysis | Trouble Shooting Manufacturing | Quality System Methodologies | Corrective & Preventative Action Processes | Operations l Production Analysis | Production Metrics | Visio | MS Project & Outlook | QAD MFG-Pro | SAP l Trackwise | Mindjet Mind Manager | IDEA
Seal Beach , Ca, Us
Responsible for scheduling and monitoring activities related to logistics and manufacturing in support of the commercial and clinical manufacturing process. Facilitated and trained for effective working relationships with internal and external customers to ensure schedules are maintained within process and logistical constraints.• Developed and maintained final product schedule during increased business and maintained 100 percent scheduling success rate.• Successfully solved discrepancies with the master schedule by communicating schedule changes to operators, and the Quality and Plant Operations team thereby maintaining a 0% schedule conflict.• Used professional concepts in accordance with company objectives to solve complex problems in creative and effective ways.• Created KPI metrics for risk mitigation and operations management.Skills & Experience Pharmaceutical Parenteral Production | Biopharmaceutical Immunotherapy Production | Planning Supply Chain | Business Process Excellence | Scheduling | Reporting | Analysis | Trouble Shooting Manufacturing | Quality System Methodologies | Corrective & Preventative Action Processes | Operations l Production Analysis | Production Metrics | Visio | MS Project & Outlook | QAD MFG-Pro | SAP l Trackwise | Mindjet Mind Manager | IDEA
Ingelheim Am Rhein, Rhineland-Palatinate, De
Data resource analyst for projects. Completed business case development, requirements definitions, project scoping, time and resource estimating and, status reporting. • Lead Role for implementation of the Balanced Scorecard approach. Assisted business areas with identifying key objectives, measures, targets, initiatives, and goals. Created metrics for strategic objectives.• Provided business and process engineering analysis for simple and complex processes and systems: Notable projects included plant capacity analysis, product equipment and BOM streamlining, and lyophilization freeze dryer capacity analysis and process optimization.• Supported FDA and EMEA regulatory inspections, preparations and corrective actions as needed.Skills & Experience Pharmaceutical Parenteral Production | Biopharmaceutical Immunotherapy Production | Planning Supply Chain | Business Process Excellence | Scheduling | Reporting | Analysis | Trouble Shooting Manufacturing | Quality System Methodologies | Corrective & Preventative Action Processes | Operations l Production Analysis | Production Metrics | Visio | MS Project & Outlook | QAD MFG-Pro | SAP l Trackwise | Mindjet Mind Manager | IDEA
Ingelheim Am Rhein, Rhineland-Palatinate, De
Served as a business partner to the Plant Manufacturing and Plant Operations.• Implemented efficiency programs resulting in average yearly savings of 450k (blue dollars), 3200 machine hours and 12,500 cumulative employee hours. >Conducted workshops and training for the purpose of identifying metrics, mapping process flow, and creating measurement tools. Provide ongoing coaching in efficiency program principles where required. >Applied efficiency processes and tools to targeted manufacturing production departments. Integrate and adapt processes into current environment where possible. >Structured and Applied Efficiency Programs and integrated tools to analyze and improve business processes. Developed, implemented and used metrics to measure progress. >Developed and implemented communication framework for the monthly and yearly reporting of progress and results within the organization. Reported progress as required to Corporate.Skills & Experience Pharmaceutical Parenteral Production | Biopharmaceutical Immunotherapy Production | Planning Supply Chain | Business Process Excellence | Scheduling | Reporting | Analysis | Trouble Shooting Manufacturing | Quality System Methodologies | Corrective & Preventative Action Processes | Operations l Production Analysis | Production Metrics | Visio | MS Project & Outlook | QAD MFG-Pro | SAP l Trackwise | Mindjet Mind Manager | IDEA
Ingelheim Am Rhein, Rhineland-Palatinate, De
Translated forecasted and hard demand from Generic, Contract and Contract Clinical requirements into plant production schedule. Managed the coordination of the activities of multiple departments (Documentation, Materials, Regulatory, Product Development, Contract, and QA/QO) to ensure timely creation and execution of the production schedule.• Enhanced companywide communication tool and framework for the translation of MRP requirements for 12 Week forecasted production schedule.• Created product cascade profiles for the reduction of required set-ups, changeovers, and positive inventory build. • Proven record for minimized downtime and 100% utilization of labor workforce.Skills & ExperiencePharmaceutical Parenteral Production | Biopharmaceutical Immunotherapy Production | Planning Supply Chain | Business Process Excellence | Scheduling | Reporting | Analysis | Trouble Shooting Manufacturing | Quality System Methodologies | Corrective & Preventative Action Processes | Operations l Production Analysis | Production Metrics | Visio | MS Project & Outlook | QAD MFG-Pro | SAP l Trackwise | IDEA
Quick answers generated from the profile data available on this page.
Derek Floyd works for Self-employed.
Derek Floyd is listed as Senior Manager | Pharmaceutical | Bio-Pharmaceutical | Production Scheduling | Continuous Process Improvement | Supply Chain| Project Management | Planning | Production Operations | Performance Metrics KPIs at Self-employed.
AeroLeads has found 1 work email signal at @serestherapeutics.com for Derek Floyd at Self-employed.
AeroLeads has found 2 phone signal(s) with area code 425 for Derek Floyd at Self-employed.
Derek Floyd is based in Aliso Viejo, California, United States while working with Self-employed.
Derek Floyd has worked for Self-Employed, Seres Therapeutics, Bachem, Avid Bioservices Inc, and Dendreon.
You can use AeroLeads to view verified contact signals for Derek Floyd at Self-employed, including work email, phone, and LinkedIn data when available.
Derek Floyd holds Bachelor Of Business Administration (Bba), Minor - Information Systems from Cleveland State University.
Derek Floyd is listed with skills including Customer Service, Scheduling, Production, Pharmaceuticals, Fda, Sop, Program Management, and Manufacturing.
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