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GEHC - Process Engineer III

In Massachusetts / United States

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GEHC - Process Engineer III   

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JOB TITLE:

GEHC - Process Engineer III

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

Marlborough Massachusetts / United States

JOB DESCRIPTION:

Description: max billBR (*feel free to submit over max rate for the rate candidate) max mark up 1.48 cytiva BIOPROCESS ENGINEER - PROCESS DESIGN MARLBOROUGH, MA onsite Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes. We are looking for a Bioprocess Engineer - Process Design to work with our Enterprise Solutions Process and System Design (P&SD) team. Do you have a passion for Process Engineering? Then we would love to hear from you. What you ll do Process Designer will support the process design efforts for biopharmaceuticals, lactoferrin and food products manufacturing, and ensure optimal outcomes to support the customer application and manufacturing operation, in compliance with applicable regulatory requirements. She/He will provide the necessary technical input to support/enable the design and development of the manufacturing suite layouts, process equipment design, process equipment layout, clean utility requirements. Process Designer will be responsible for process design documentations and operational estimates such as Basis of Design, Mass/volume Balance, Equipment List, Process Flow Diagrams (PFDs), Production Schedule, Clean Utilities Estimates, Cost of Goods Analysis, Process Definition, etc. Support customer meetings by providing process understanding from pilot scale operation, technology transfer, large scale manufacturing and facility design experience. Provide Process Design & Engineering support for the Enterprise Project Team. Work closely with the Enterprise Solutions Project Manager to support the Enterprise Solutions project specific design development, documentation and execution in alignment with the project scope and schedule. Provide design input, support and recommendations as needed with qualification test review and verification and during field execution, commissioning and qualification testing. Assure compliance with the Cytiva Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position. Work closely with Customer's Subject Matter Experts (SMEs) to ensure continuous exchange of critical and technical information needed to execute design activities on time. Work closely with Engineering partner companies during Conceptual, Basic design development, installation, commissioning and testing phase to ensure suitability, applicability and accuracy of Engineering partner designs, calculations, drawings; ensure they are in alignment with customer requirements. Complete all planned Quality & Compliance training within defined deadlines. Identify and report any quality or compliance concerns and take immediate corrective action as required. Work closely with System Designers for the generation of URSs and GSs, and ensure the transfer of critical equipment requirement specification, design meets customer and process needs, and the single-use equipment layout is optimized for the customer facility. Approximately 10-30% travel depending on project specifics and geographic location. Who you are BS or MS degree in biochemical / chemical engineering or in a related engineering/life Science discipline or equivalent experience in Biopharma, Lactoferrin and Food industries.Page 2 / 2 Minimum of 3 years of relevant bioprocess experience. 1 years of direct experience working in a pilot plant or GMP manufacturing facility. Experience in manufacturing of monoclonal antibodies, viral vectors, pDNA and other biologics. Working knowledge of pharmaceutical, Lactoperoxidase / lactoferrin separation, and other biotech processes, equipment hardware, and single use technology. Knowledge of biologics CMC, cGMP manufacturing requirements. Working knowledge of pharmaceutical/biotech processes, equipment hardware, and single use technology. Knowledge of biologics CMC, cGMP manufacturing requirements. Experience in working with cross functional teams. Experience with Visio, MS Project, SuperPro, and AutoCAD. Technical understanding of automation systems used in the biopharma (Delta V, PLC, PI, etc.). Disposable technology design and application experience. Detail oriented, excellent at critical analysis and problem solving. Comfortable working in global business environment. Structured, Organized, Analytical, Team oriented. Fluent in English both verbally and in writing. Who we are Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you ll feel right at home here. If you re flexible, curious and relentless, you ll belong. If you are excited about a global culture, this can be the place to further your career. Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page! Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients. Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world. Qualification Rating Must Have Healthcare Driving record verification? No Education verification? No GEHC Magnetic Resonance Employee Questionnaire for Metallic Foreign Body and Electronic Devices? No Pre-Identified Candidate Question Answer Have you already identified a candidate? No Pre-Identified Candidate result End Pre-Identified Candidate

Position Details

POSTED:

Oct 10, 2022

EMPLOYMENT:

INDUSTRY:

SNAPRECRUIT ID:

S16204864071102211

LOCATION:

Massachusetts / United States

CITY:

Marlborough

Job Origin:

CEIPAL_ORGANIC_FEED

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Description: max billBR (*feel free to submit over max rate for the rate candidate) max mark up 1.48 cytiva BIOPROCESS ENGINEER - PROCESS DESIGN MARLBOROUGH, MA onsite Help us improve access to life-changing therapies that can transform human health We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes. We are looking for a Bioprocess Engineer - Process Design to work with our Enterprise Solutions Process and System Design (P&SD) team. Do you have a passion for Process Engineering? Then we would love to hear from you. What you ll do Process Designer will support the process design efforts for biopharmaceuticals, lactoferrin and food products manufacturing, and ensure optimal outcomes to support the customer application and manufacturing operation, in compliance with applicable regulatory requirements. She/He will provide the necessary technical input to support/enable the design and development of the manufacturing suite layouts, process equipment design, process equipment layout, clean utility requirements. Process Designer will be responsible for process design documentations and operational estimates such as Basis of Design, Mass/volume Balance, Equipment List, Process Flow Diagrams (PFDs), Production Schedule, Clean Utilities Estimates, Cost of Goods Analysis, Process Definition, etc. Support customer meetings by providing process understanding from pilot scale operation, technology transfer, large scale manufacturing and facility design experience. Provide Process Design & Engineering support for the Enterprise Project Team. Work closely with the Enterprise Solutions Project Manager to support the Enterprise Solutions project specific design development, documentation and execution in alignment with the project scope and schedule. Provide design input, support and recommendations as needed with qualification test review and verification and during field execution, commissioning and qualification testing. Assure compliance with the Cytiva Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position. Work closely with Customer's Subject Matter Experts (SMEs) to ensure continuous exchange of critical and technical information needed to execute design activities on time. Work closely with Engineering partner companies during Conceptual, Basic design development, installation, commissioning and testing phase to ensure suitability, applicability and accuracy of Engineering partner designs, calculations, drawings; ensure they are in alignment with customer requirements. Complete all planned Quality & Compliance training within defined deadlines. Identify and report any quality or compliance concerns and take immediate corrective action as required. Work closely with System Designers for the generation of URSs and GSs, and ensure the transfer of critical equipment requirement specification, design meets customer and process needs, and the single-use equipment layout is optimized for the customer facility. Approximately 10-30% travel depending on project specifics and geographic location. Who you are BS or MS degree in biochemical / chemical engineering or in a related engineering/life Science discipline or equivalent experience in Biopharma, Lactoferrin and Food industries.Page 2 / 2 Minimum of 3 years of relevant bioprocess experience. 1 years of direct experience working in a pilot plant or GMP manufacturing facility. Experience in manufacturing of monoclonal antibodies, viral vectors, pDNA and other biologics. Working knowledge of pharmaceutical, Lactoperoxidase / lactoferrin separation, and other biotech processes, equipment hardware, and single use technology. Knowledge of biologics CMC, cGMP manufacturing requirements. Working knowledge of pharmaceutical/biotech processes, equipment hardware, and single use technology. Knowledge of biologics CMC, cGMP manufacturing requirements. Experience in working with cross functional teams. Experience with Visio, MS Project, SuperPro, and AutoCAD. Technical understanding of automation systems used in the biopharma (Delta V, PLC, PI, etc.). Disposable technology design and application experience. Detail oriented, excellent at critical analysis and problem solving. Comfortable working in global business environment. Structured, Organized, Analytical, Team oriented. Fluent in English both verbally and in writing. Who we are Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you ll feel right at home here. If you re flexible, curious and relentless, you ll belong. If you are excited about a global culture, this can be the place to further your career. Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page! Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who are dedicated to our mission to help us improve access to life-changing therapies that transform human health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients. Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world. Qualification Rating Must Have Healthcare Driving record verification? No Education verification? No GEHC Magnetic Resonance Employee Questionnaire for Metallic Foreign Body and Electronic Devices? No Pre-Identified Candidate Question Answer Have you already identified a candidate? No Pre-Identified Candidate result End Pre-Identified Candidate


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