Product Engineer Salary in Connecticut, USA

Principal ResponsibilitiesProvide technical support to the Sales force in the areas of bearing design, design improvements, customer support, production support and review of new applications. Works with customers to resolve technical problems and makes technical presentations with the Sales Engineers at target accounts. Review of new applications and provide technical solutions to ensure product performance. Responsible for the conceptual design engineering of new products, special products and contribute to the improvement of existing products and manufacturing methods to meet customer demands. Technical consultant on product design, application and service problems, quality deviations and material and parts substitution. Assists in the technical education of sales trainees and personnel of other departments. Member of the Material Review Board which is responsible for the disposition of all nonconforming product and materials. Functions as an engineering consultant to manufacturing on problems related to the manufacture of the company's products. Provides product design requirements to mechanical designers assigned to specific projects and assures that all detail drawings are in conformance to the requirements and technical specifications. Responsible for establishing new products into the MRP system and creating the associated Bill-of-Material. Responsible for approving new product designs and releasing designs to manufacturing Supports lean enterprise activities.

Title: QA Automation Engineer- Mostly remoteLocation: Hartford, CT, USALength: Long termRestriction: W2 or C2CDescription:*** Hybrid *** Webcam interview very long term project initial PO for 1 year with multiyear extensions *** 20% onsite*** Candidate Must Be Local/relocate.*** Due to security Candidate must be a U.S. Citizen or Permanent Resident ***SCOPE OF WORK:The agency needs the service of 1 HANDS ON QA Automation Engineer. The candidate will serve in the capacity of a QA Automation Engineer, will follow a well defined vision of how IT and the business aligns and make sure that everyone is following the same principles, methodologies, and support activities per the direction of agency management. The specific focus of this candidate will be to ensure that functional requirements are met whilst also ensuring that service qualities (Performance, scalability, extensibility, maintainability, security, interoperability) for now and for the future are achievable. In addition, this role is responsible for reviewing and improving on existing systems, making use of new technologies and methodologies to seek continual improvement for existing systemsSpecific Services Required:In the role of the QA Automation Tester, the following services are required:Follow the core technology and architecture for automated testing of large scale distributed systems, midrange to client server and n tier e commerce applications and solutions.Follow specifications to automate the testing of applications.Work on all test automation components of solution and create/maintain required technical documentation.Follow developed strategies for end to end system testing.Assist in all testing processes involving the migration and integration of new and legacy technologies.Excellent communication, presentation, collaboration, and interpersonal skills.Demonstrated ability to deliver business and technical value.Must be very organized, pro active, and self directed. Must be able to perform with minimal supervision.Must have very strong abstract thinking and problem solving skills.Must have very good verbal and written communication skills.Work with the Quality Assurance Manager to establish goals and release quality while meeting requirements of projects.Work with the Quality Assurance Manager to establish goals and release quality while meeting requirements of projects.Follows the testing standards and strategies and uses them correctly.Makes sure the software and system testing frameworks are in synchronization.Interface with the user(s) and sponsor(s) and all other stakeholders to determine their (evolving) needs.Follows the set standards for the automated testing software, policies, and execution.Reviews all system requirements, test scripts, test scenarios to create appropriate testing workflow. Ensures that this set of high level requirements is consistent, complete, correct, and operationally defined.Reviews software components and collaborates with development group, Product Owners, System Teams, and Operations to ensure best overall testing strategies, best practices, and techniques for automated testing.Interfaces with the design and implementation teams, so that any problems arising during QA can be resolved in accordance with the fundamental design concepts, and user needs and constraints.Collaborates on a set of acceptance test requirements, together with the project teams, and the user, which determine that all of the high level requirements have been met, especially for the computer human interface.Generates products such as unit tests, automated functional tests, regression tests, load tests, code coverage reports, and test scenario % pass/fail, ADA/508c/AWGA compliance, Cross Browser Compatibility, Mobile Compatibility.Ensures that all testing libraries and artifacts are maintained in the most current state and never allowed to become obsolete.Responsible for creating automated test case scenarios for Agile Delivery Team to meet Acceptance CriteriaREQUIRED SKILLS AND EXPERIENCE:Refer to the State contracts for IT Professional Services Agreement (22PSX0163) for experience and skill requirements for the job classification Solution Architect to fill the role. In addition, the agency requires:For this position, the candidate shares their experience and judgment with the team to plan, accomplish goals and mentors less experienced staff. In addition, the agency requires:An experience professional with demonstrating the following knowledge and skills:5+ years Experience Azure DevOps suite (Azure Boards, Azure Repos, Azure Pipelines, Azure Test Plans, Azure Artifacts) (*required)5+ years Experience in automated testing with UFT (Unified Functional Testing) and VBScript or different programing language. (*required)5+ years Experience with Automated Testing Frameworks and Manual Testing, Test Methodologies, Test Strategies and Test Beds.(*required)5+ years Experience with Agile MethodologiesExperience with Azure Test Management Tool (*required)Develop and Maintain UI, Back End, API, and Hardware Test AutomationInvolved in a minimum of two large scaled Agile software development projectsKnowledge of Testing Tools, Testing Frameworks, Continuous Integration MethodologiesKnowledge of Web Application Testing, Distributed System Testing, Performance Testing, Regression Testing, Database Testing, Mobile Testing, Security Testing, Accessibility Testing, Web Service Testing.Knowledge of .Net, SharePoint, Dynamics Web Application Hosting EnvironmentKnowledge of Data Modeling and Database Design preferredKnowledge of Application Modeling and DesignKnowledge of Service Oriented ArchitecturesExperience with automated testing in enterprise system integration projects and initiatives understanding of and experience implementing enterprise integration patterns.Thorough understanding of standard QA best practices in an Agile environment including authoring test plans and test cases, executing tests and tracking issues to closureExperience in Test Driven Development and testing tools and techniques.Object Oriented design principles and design patternsAdditional Preferred Qualifications:Experience with web automation suites e.g. SeleniumExperience with QA Functional test suites such as Azure and Unified Functional Testing.Working automated testing knowledge for C#, WCF, jQuery, XML, JSON, WebApi, SOAP, .NET, JavaScript.Testing experience with Web Services (REST, SOAP, WCF) and tools such as SOAPUI and SOAPSonar.BS in Computer science, engineering, or technology related baccalaureate degree from an accredited college or university, or commensurate experience.Experience with SalesforceExperience Microsoft SharePointExperience with .Net FrameworkKnowledge of Virtualized Hosting EnvironmentsKnowledge of .Net, SharePoint, Dynamics Web Application PerformanceKnowledge of .Net, SharePoint, Dynamics Web Application SecuritySQL

Title: QA Automation Engineer - HybridLocation: Hartford, Connecticut, USALength: Long termRestriction: W2 or C2CDescription:***Hybrid - one day per week onsite*** ** Webcam interview very long term project initial PO for 1 year with multiyear extensions *** Local or relocate*** due to security only USC or GCThe candidate will serve in the capacity of a QA Automation Engineer, will follow a well defined vision of how IT and the business aligns and make sure that everyone is following the same principles, methodologies, and support activities per the direction of agency management. The specific focus of this candidate will be to ensure that functional requirements are met whilst also ensuring that service qualities (Performance, scalability, extensibility, maintainability, security, interoperability) for now and for the future are achievable. In addition, this role is responsible for reviewing and improving on existing systems, making use of new technologies and methodologies to seek continual improvement for existing systemsSpecific Services Required:In the role of the QA Automation Tester, the following services are required:Follow the core technology and architecture for automated testing of large scale distributed systems, midrange to client server and n tier e commerce applications and solutions.Follow specifications to automate the testing of applications.Work on all test automation components of solution and create/maintain required technical documentation.Follow developed strategies for end to end system testing.Assist in all testing processes involving the migration and integration of new and legacy technologies.Excellent communication, presentation, collaboration, and interpersonal skillsDemonstrated ability to deliver business and technical value.Must be very organized, pro active, and self directed. Must be able to perform with minimal supervision.Must have very strong abstract thinking and problem solving skills.Must have very good verbal and written communication skills.Work with the Quality Assurance Manager to establish goals and release quality while meeting requirements of projects.Work with the Quality Assurance Manager to establish goals and release quality while meeting requirements of projects.Follows the testing standards and strategies and uses them correctly.Makes sure the software and system testing frameworks are in synchronization.Interface with the user(s) and sponsor(s) and all other stakeholders to determine their (evolving) needs.Follows the set standards for the automated testing software, policies, and execution.Reviews all system requirements, test scripts, test scenarios to create appropriate testing workflow. Ensures that this set of high level requirements is consistent, complete, correct, and operationally defined.Reviews software components and collaborates with development group, Product Owners, System Teams, and Operations to ensure best overall testing strategies, best practices, and techniques for automated testing.Interfaces with the design and implementation teams, so that any problems arising during QA can be resolved in accordance with the fundamental design concepts, and user needs and constraints.Collaborates on a set of acceptance test requirements, together with the project teams, and the user, which determine that all of the high level requirements have been met, especially for the computer human interfaceGenerates products such as unit tests, automated functional tests, regression tests, load tests, code coverage reports, and test scenario % pass/fail, ADA/508c/AWGA compliance, Cross Browser Compatibility, Mobile Compatibility.Ensures that all testing libraries and artifacts are maintained in the most current state and never allowed to become obsolete.Responsible for creating automated test case scenarios for Agile Delivery Team to meet Acceptance CriteriaREQUIRED SKILLS AND EXPERIENCE:Refer to the State contracts for IT Professional Services Agreement (22PSX0163) for experience and skill requirements for the job classification Solution Architect to fill the role. In addition, the agency requires:For this position, the candidate shares their experience and judgment with the team to plan, accomplish goals and mentors less experienced staff. In addition, the agency requires:An experience professional with demonstrating the following knowledge and skills:5+ years Experience Azure DevOps suite (Azure Boards, Azure Repos, Azure Pipelines, Azure Test Plans, Azure Artifacts) (*required)5+ years Experience in automated testing with UFT (Unified Functional Testing) and VBScript or different programing language. (*required)5+ years Experience with Automated Testing Frameworks and Manual Testing, Test Methodologies, Test Strategies and Test Beds.(*required)5+ years Experience with Agile MethodologiesExperience with Azure Test Management Tool (*required)Develop and Maintain UI, Back End, API, and Hardware Test AutomationInvolved in a minimum of two large scaled Agile software development projectsKnowledge of Testing Tools, Testing Frameworks, Continuous Integration MethodologiesKnowledge of Web Application Testing, Distributed System Testing, Performance Testing, Regression Testing, Database Testing, Mobile Testing, Security Testing, Accessibility Testing, Web Service Testing.Knowledge of .Net, SharePoint, Dynamics Web Application Hosting EnvironmentKnowledge of Data Modeling and Database Design preferredKnowledge of Application Modeling and DesignKnowledge of Service Oriented ArchitecturesExperience with automated testing in enterprise system integration projects and initiatives understanding of and experience implementing enterprise integration patterns.Thorough understanding of standard QA best practices in an Agile environment including authoring test plans and test cases, executing tests and tracking issues to closureExperience in Test Driven Development and testing tools and techniques.Object Oriented design principles and design patternsAdditional Preferred Qualifications:Experience with web automation suites e.g. SeleniumExperience with QA Functional test suites such as Azure and Unified Functional Testing.Working automated testing knowledge for C#, WCF, jQuery, XML, JSON, WebApi, SOAP, .NET, JavaScript.Testing experience with Web Services (REST, SOAP, WCF) and tools such as SOAPUI and SOAPSonar.BS in Computer science, engineering, or technology related baccalaureate degree from an accredited college or university, or commensurate experience.Experience with SalesforceExperience Microsoft SharePointExperience with .Net FrameworkKnowledge of Virtualized Hosting EnvironmentsKnowledge of .Net, SharePoint, Dynamics Web Application PerformanceKnowledge of .Net, SharePoint, Dynamics Web Application SecuritySQLRequired Skills:Microsoft SQL Server 7/9 yeras

Senior Product Engineer - RSTThis position will be based out of Medtronic's campus in North Haven, CT and reports to the Engineering Manager of the Consumables Product Engineering Team in Released Product Engineering Organization. The Senior Product Engineer will coordinate the cross-functional team to deliver hardware design changes for products used for Robotic Surgery Hugo.Outstanding written and verbal communication skills are critical to success in this role, as is the ability to thrive in a fast-paced environment. You will work closely with mechanical, electrical and verification engineering teams to plan the technical details of the hardware change, while coordinating with project management, manufacturing, marketing and quality to meet timelines and business needs. This person will be able to dive in deep technically, but also able to see the broader needs of the business and the Robotics Surgical Technologies business unit.Careers that Change LivesYou will join a world class team of mechanical, electrical and software engineers responsible for further development and enhancement of the globally launched Robotic Assisted Surgery platform: https://www.medtronic.com/covidien/en-us/robotic-assisted-surgery/hugo-ras-system.htmlImpact patient outcomes. Come for a job, stay for a career.In the Robotic Surgical Technologies, part of Medtronic's Surgical Operating Unit, we believe patients around the world deserve access to quality care and improved outcomes. We strive to expand global access to care and reduce variability through robotic and analytics solutions.A Day in the Life Drive execution of hardware design changes or enhancements proposed for Hugo Consumables Product. Be the key central communications point for sustaining related project activity. Track deliverables from internal and external teams against product design change requirements. Anticipate, identify, and provide technical solutions to a wide range of difficult problems. Participate in investigations leading to problem resolution. Mitigate production and manufacturing risks by identifying areas of opportunity and executing improvement projects. Drive technical changes related to product component & assembly, with knowledge of process and finished product impact. Assess timeline impacts against project schedule. Work with engineers to develop a deep understanding of the technological underpinnings of the system. Conducts project management tasks & documentation with design controls and risk analysis in accordance with established SOPs. Lead or coordinate with peers on product investigations that drive design and process improvement efforts. Participate in new process development activities at supplier base and contract sites, along with qualification efforts to implement new product materials or process changes. Incorporate required regulatory standards (FDA, ISO) in developmental and/or sustaining engineering projects including written protocols, test methods, assembly processes and the Design History File. Prepare reports, presentations and spreadsheets of an analytical and interpretative nature using statistical data analysis methods Responsible for production support engineering with respect to testing methods, procedures, and problems; device specification and yield problems; minor redesign of devices and masks; analysis of customer returns; supplier related engineering changes and optimizing device production relative to cost constraints. Assumes responsibility for device and/or internally produced or externally purchased components after transfer into high-volume production and usually responsible for entire device manufacturing operations other than wafer fabrication. May assist customer in device usage problems or customer testing of complex devices. Additional tasks as assigned Must Have: Minimum Requirements Bachelor's degree with 4 years of engineering experience OR An advanced degree with 2 years of engineering experience Nice to Have Knowledge of medical device manufacturing documentation for product release Knowledge of project management tools Outstanding verbal and written communication skills Strong leadership skills Comfortable working in a fast paced, cross disciplinary environment Ability to discuss technical details with engineering staff, the ideal candidate will have a strong engineering and product development background. Able to work with minimal direction towards completing project tasks Takes initiative in keeping current with technology developments in specialized area. Working knowledge of applicable FDA and ISO standards. Thorough understanding of engineering practices, product safety and root cause analysis. Working knowledge of Design for Six Sigma, Failure Mode Effects Analysis, Statistical Analysis methods, and Design of Experiments. Effective in written and oral communication; experienced in report writing and development of presentations. Good understanding of structured product development (requirements-driven engineering, documentation, rigorous verification, etc.) Engineering verification test development and execution Understanding and experience with system reliability testing and service. About MedtronicTogether, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future.Physical Job RequirementsThe physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager, recruiter or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)CompensationA commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Learn more about our benefits here .This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) on page 6 here .The provided base salary range is used nationally (except in certain CA locations).The rate offered is compliant with federal/local regulations and may vary by experience,certification/education, market conditions, location, etc.

Senior Product Engineer, R&D RPE - Robotic Surgical TechnologiesThis position will be based out of Medtronic's campus in North Haven, CT and reports to the Engineering Manager of the Capital Product Engineering Team in Released Product Engineering Organization. The Senior Product Engineer will coordinate the cross-functional team to deliver hardware design changes for products used for Robotic Surgery Hugo.Outstanding written and verbal communication skills are critical to success in this role, as is the ability to thrive in a fast-paced environment. You will work closely with mechanical, electrical and verification engineering teams to plan the technical details of the hardware change, while coordinating with project management, manufacturing, marketing and quality to meet timelines and business needs. This person will be able to dive in deep technically, but also able to see the broader needs of the business and the Robotics Surgical Technologies business unit.Location: North Haven, CTOperating UnitIn the Robotic Surgical Technologies, part of Medtronic's Surgical Operating Unit, we believe patients around the world deserve access to quality care and improved outcomes. We strive to expand global access to care and reduce variability through robotic and analytics solutions.You will join a world class team of mechanical, electrical and software engineers responsible for further development and enhancement of the globally launched Robotic Assisted Surgery platform: https://www.medtronic.com/covidien/en-us/robotic-assisted-surgery/hugo-ras-system.htmlCareers that Change LivesOne of the many ways we foster our inclusive environment is through our Diversity Networks and Employee Resource Groups. Our Diversity Networks leaders are teams appointed by our CEO. They champion programs and policies that advance more women and ethnically diverse employees into leadership roles. In the U.S., we have an African Descent Network, Asian Descent Network and Hispanic Descent Network. The PRIDE network and the Medtronic Women's Network are global communities. These unique networks are critical to ensuring the voice of the community is heard. They work closely with senior leaders and HR to create programs to further the advancement of diverse employees.A Day in the Life Lead cross functional team to drive execution of hardware design changes or enhancements proposed for Hugo Capital Product. Be the key central communications point for sustaining related project activity. Track deliverables from internal and external teams against product design change requirements. Anticipate, identify, and provide technical solutions to a wide range of difficult problems. Understand root cause analysis tools with ability to participate in investigations leading to problem resolution. Mitigate production and manufacturing risks by identifying areas of opportunity and executing improvement projects. Ability to drive technical changes related to product component & assembly, with knowledge of process and finished product impact. Assess timeline impacts against project schedule. Work with engineers to develop a deep understanding of the technological underpinnings of the system. Conducts project management tasks & documentation with design controls and risk analysis in accordance with established SOPs. Lead or coordinate with peers on product investigations that drive design and process improvement efforts. Participate in new process development activities at supplier base and contract sites, along with qualification efforts to implement new product materials or process changes. Incorporate required regulatory standards (FDA, ISO) in developmental and/or sustaining engineering projects including written protocols, test methods, assembly processes and the Design History File. Prepare reports, presentations and spreadsheets of an analytical and interpretative nature using statistical data analysis methods. Responsible for production support engineering with respect to testing methods, procedures, and problems; device specification and yield problems; minor redesign of devices and masks; analysis of customer returns; supplier related engineering changes and optimizing device production relative to cost constraints. Assumes responsibility for device and/or internally produced or externally purchased components after transfer into high-volume production and usually responsible for entire device manufacturing operations other than wafer fabrication. Additional tasks as assigned Must Have: Minimum Requirements Bachelor's degree with 4+ years of engineering experience OR An advanced degree with 2+ years of engineering experience Nice to Have 5+ years of medical device experience Advanced degree in engineering Experience with medical device hardware design changes Experience with robotic devices Strong leadership skills Knowledge of medical device manufacturing documentation for product release Knowledge of project management tools Outstanding verbal and written communication skills Comfortable working in a fast paced, cross disciplinary environment Ability to discuss technical details with engineering staff, the ideal candidate will have a strong engineering and product development background. Able to work with minimal direction towards completing project tasks Takes initiative in keeping current with technology developments in specialized area. Working knowledge of applicable FDA and ISO standards. Thorough understanding of engineering practices, product safety and root cause analysis. Working knowledge of Design for Six Sigma, Failure Mode Effects Analysis, Statistical Analysis methods, and Design of Experiments. Effective in written and oral communication; experienced in report writing and development of presentations. Good understanding of structured product development (requirements-driven engineering, documentation, rigorous verification, etc.) Engineering verification test development and execution Understanding and experience with system reliability testing and service. About MedtronicTogether, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future.Physical Job RequirementsThe physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager, recruiter or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)

Embedded controllers - Selection of microcontrollers suitable for the application. Functions for serial and network communications, internal status monitoring, failure logging and closed loop controls.Software development in C for embedded controls and PC software tools with Visual Studio. Microchip Technology processors and development tools are primarily used.Power circuit designs include IGBT bridge and driver circuits for voltages up to rectified 575 VAC 3 phase power with a clear understanding of the materials and spacing requirements of the circuit board. Knowledge of passive and active power factor correction methods and circuits is key for these products. A good understanding of power grid transients and anomalies is key in understanding how do design for robustness.Design of switch mode power supplies with the analysis of system power requirements including the possible transients and anomalies of mains power. LTspice is the mail tool used for simulation of power supplies as well as general analog analysis.In conjunction with the product research and designs, there will be development of test fixtures and procedures for the evaluation of the electronics for accuracy, robustness and reliability. Hardware and software is developed for creating test conditions as well as data logging of electrical signals and thermal stresses.Circuit analysis should include reliability, component derating, thermal and component stress. The analysis data is used in design reviews, design verification and FMEA.There should be familiarity with regulatory safety and EMC standards for industrial and residential applications. (UL, FCC, NEBS, IEC, etc.) Tracking of tests to log the progress of compliance for status updates.This position is part of a project team including a PCB design engineer, local electrical engineers, global electrical engineers, applications engineers, mechanical engineers and manufacturing engineers. The product development involves all stages from conceptualization to production as well as a broad range of understanding from EMS, mechanical, production, thermal and airflow issues. Excellent communication skills are needed to keep team members informed and the projects progressing as well as good listening skills to properly understand issues. The ideal candidate should be self-motivated to understand these areas and broad these skills.Plan and track program development, project progress and schedules. The use of MS Project is key in this role. Schedules and progress will regularly be presented with MS PowerPoint.There will be collaboration of ideas and designs with German divisions, and travel may be required at times for training and meetings.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.Bachelor's Degree in Electrical Engineering5+ Years of experience in circuit designEmbedded Controllers and Software Development in CPower Circuit DesignCircuit Analysis (FMEA)EMC Standards KnowledgeProject Management experience (Experience with MS Project is key)

This is what you will do: This position will lead research, design and implement scientific studies to enable the drug product (DP) process development, characterization, clinical manufacturing, and commercial validation of parenteral/injectable biologic products. Lead and support execution of stability studies, data processing, compiling and presentation of results supporting late-stage clinical activities as well as preparation for PPQ. Develop a variety of manufacturing unit operations including, drug substance (DS) freeze/thaw, compounding/mixing, sterile filtration, drug product filling of vials/syringes, visual inspection, and DS/DP transportation. A general understanding of protein chemistry and/or the ability to run biopharmaceutical assays in a laboratory is preferred.The role will lead manufacturing technology transfer activities in preparation for DS and DP PPQs, sending/receiving site process gap analysis, process FMEAs (failure mode and effects analysis), change control owner/leader, master batch record review, as well as leading at-scale/full scale process development studies, and authoring protocols, and reports. In addition, will support deviation investigations, change controls, and CAPAs using electronic Quality system. The candidate will also provide clinical and commercial manufacturing site support including but not limited to periodic meetings, action item owner, and in-person on-site manufacturing support. Interact regularly with multi-functional staff from Analytical Sciences & Quality Control, Drug Substance Process Development, Manufacturing Technical Services, Quality Assurance, and/or CMC Regulatory Affairs to support progress of the program and preparation of source documentation supporting BLA.You will be responsible for: Own the design and implement studies for Alexion pharmaceuticals' clinical drug candidates and commercial products, support tech transfer activities for internal manufacturing and contract manufacturing sitesLead progression of projects with multi-functional collaborators, as well as understand the implications of project activities and decisions with minimal directionPrioritizing multiple tasks and projects independently and as part of the teamAuthor SOPs, study protocols and technical reportsParticipate in multi-functional development teams representing Injectable Drug Product DevelopmentMaintain knowledge of current trends in drug product manufacturing processes, manufacturing equipment and single use systems as well as associated global regulatory expectations and scientific principles and theories. Train other peers as assigned in areas of expertiseActively participate in department and team meetings including assuming ownership and delivering on assign action itemsDevelop presentations for meetings with internal and external partnersYou will need to have:Bachelor's degree in Chemical Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, or relevant Engineering/Life Sciences field with 4+ years of relevant experience or Master's degree with 3+ years of relevant work experienceDedicated initiative to find resolution for technical challengesExcellent interpersonal, collaborative and communication skillsThe duties of this role are conducted in a lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video and electronic messaging; engage in problem solving and non-linear thought, analysis and dialogue; collaborate with others; maintain general availability during standard business hours.We would prefer for you to have:Scientific and practical knowledge of protein biochemistry and/or drug product process developmentPrevious experience in bio-therapeutics development as well as relevant knowledge of cGMP and Quality expectations for PPQs and BLAScientific understanding of protein stability, thermodynamics, mechanism of protein degradation, bio-therapeutics drug formulation development and analytical tools used to test formulations is a plusHigh level proficiency in MS Office software including Word, Excel, Outlook, Visio, and PowerPointExpectation of working in the office 4 days a week statement: When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of four days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world!AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

This is what you will do: This position will lead research, design and implement scientific studies to enable the drug product (DP) process development, characterization, clinical manufacturing, and commercial validation of parenteral/injectable biologic products. Lead and support execution of stability studies, data processing, compiling and presentation of results supporting late-stage clinical activities as well as preparation for PPQ. Develop a variety of manufacturing unit operations including, drug substance (DS) freeze/thaw, compounding/mixing, sterile filtration, drug product filling of vials/syringes, visual inspection, and DS/DP transportation. A general understanding of protein chemistry and/or the ability to run biopharmaceutical assays in a laboratory is preferred.The role will lead manufacturing technology transfer activities in preparation for DS and DP PPQs, sending/receiving site process gap analysis, process FMEAs (failure mode and effects analysis), change control owner/leader, master batch record review, as well as leading at-scale/full scale process development studies, and authoring protocols, and reports. In addition, will support deviation investigations, change controls, and CAPAs using electronic Quality system. The candidate will also provide clinical and commercial manufacturing site support including but not limited to periodic meetings, action item owner, and in-person on-site manufacturing support. Interact regularly with multi-functional staff from Analytical Sciences & Quality Control, Drug Substance Process Development, Manufacturing Technical Services, Quality Assurance, and/or CMC Regulatory Affairs to support progress of the program and preparation of source documentation supporting BLA.You will be responsible for: Own the design and implement studies for Alexion pharmaceuticals' clinical drug candidates and commercial products, support tech transfer activities for internal manufacturing and contract manufacturing sitesLead progression of projects with multi-functional collaborators, as well as understand the implications of project activities and decisions with minimal directionPrioritizing multiple tasks and projects independently and as part of the teamAuthor SOPs, study protocols and technical reportsParticipate in multi-functional development teams representing Injectable Drug Product DevelopmentMaintain knowledge of current trends in drug product manufacturing processes, manufacturing equipment and single use systems as well as associated global regulatory expectations and scientific principles and theories. Train other peers as assigned in areas of expertiseActively participate in department and team meetings including assuming ownership and delivering on assign action itemsDevelop presentations for meetings with internal and external partnersYou will need to have:Bachelor's degree in Chemical Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, or relevant Engineering/Life Sciences field with 4+ years of relevant experience or Master's degree with 3+ years of relevant work experienceDedicated initiative to find resolution for technical challengesExcellent interpersonal, collaborative and communication skillsThe duties of this role are conducted in a lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video and electronic messaging; engage in problem solving and non-linear thought, analysis and dialogue; collaborate with others; maintain general availability during standard business hours.We would prefer for you to have:Scientific and practical knowledge of protein biochemistry and/or drug product process developmentPrevious experience in bio-therapeutics development as well as relevant knowledge of cGMP and Quality expectations for PPQs and BLAScientific understanding of protein stability, thermodynamics, mechanism of protein degradation, bio-therapeutics drug formulation development and analytical tools used to test formulations is a plusHigh level proficiency in MS Office software including Word, Excel, Outlook, Visio, and PowerPointExpectation of working in the office 4 days a week statement: When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of four days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world!Date Posted26-Apr-2024Closing Date30-Jul-2024Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact [email protected]. Alexion participates in E-Verify.AstraZeneca requires all US employees to be fully vaccinated for COVID-19 but will consider requests for reasonable accommodations as required by applicable law.

Product Engineer II, RPE - Surgical RoboticsThe RPE Engineer will work closely with the project management office, Medtronic design engineers, and our contract manufacturing sites. You will be able to dive in deep technically, and lead design change initiatives on the capital equipment products used in Robotic Surgery. Outstanding written and verbal communication skills are critical to success in this role, as is the ability to thrive in a fast-paced environment.Location: This position will be based out of Medtronic's campus in North Haven CT.Careers that Change LivesYou will be a key member of Medtronic's Robotic Surgical Technologies R&D - Released Product Engineering (RPE) team, working to support the design of our launched Hugo TM robot. You will be a critical member of projects related to cost down, component end-of-life issues, field complaint resolution implementation, and more, in a very visible and fast-paced role.Impact patient outcomes. Come for a job, stay for a career.Medtronic strives to enable earlier diagnosis, better treatment, faster complication-free recovery, and enhanced patient outcomes through less invasive surgical solutions.The Surgical operating unit set the standard for Minimally Invasive Surgery (MIS) by creating innovative surgical products and services that focus on obesity and diseases and conditions of the gastrointestinal tract, lung, abdominal wall, pelvic region, and the head and neck.A Day in the Life Lead change development plan for design changes to Hugo Be central communication point for all project related activity Work with engineers to develop a deep understanding of the technological underpinnings of the system Assess timeline impacts against project schedule Perform action item follow up Create purchase requisitions Deliver meeting minutes Responsible for production support engineering with respect to testing methods, procedures, and problems; device specification and yield problems; minor redesign of devices and masks; analysis of customer returns; supplier related engineering changes and optimizing device production relative to cost constraints. Assumes responsibility for device and/or internally produced or externally purchased components after transfer into high-volume production and usually responsible for entire device manufacturing operations other than wafer fabrication. May assist customer in device usage problems or customer testing of complex devices. Additional tasks as assigned Must Have: Minimum Requirements Bachelor's Degree with 2 years of engineering experience OR An advanced degree with 0 years of engineering experience Nice to Have Bachelor's Degree in Mechanical Engineering, Robotics, Electrical Engineering, or related field required Previous product engineering experience with Medtronic Experience with highly regulated and/or safety-critical systems (medical device experience strongly preferred) Outstanding verbal and written communication skills Strong leadership skills Comfortable working in a fast passed, cross disciplinary environment Ability to discuss technical details with engineering staff, the ideal candidate will have strong engineering and product development skills. Ability to create and track a project budget and timeline About MedtronicTogether, we can change healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future.Physical Job RequirementsThe physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager, recruiter or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. (ADA-United States of America)CompensationA commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Learn more about our benefits here .This position is eligible for a short-term incentive plan. Learn more about Medtronic Incentive Plan (MIP) on page 6 here .The provided base salary range is used nationally (except in certain CA locations).The rate offered is compliant with federal/local regulations and may vary by experience,certification/education, market conditions, location, etc.

Why Open: Additional Support NeededPosition: Product OwnerLocation: 100% onsite- Stamford, CTLength: Contract Thru EOY, possible extensionPay Rate: 45-50/hrInterview Process: (1st 30 min conversation w/ director, 2nd call with VP)Must Haves:4+ years of product owner/ analyst experienceStrong background within gathering and writing requirementsAbility to work with both technical and non-technical people: technical people being QAs, Engineers, ITStrong experience w/ journey mapping:gathering/writing requirementsfollowing customer experiencecreating process flowsStrong experience creating PowerPoint decks: presented at executive levelExperience working within both an Agile & Waterfall environmentGood communication & personalityPlusses:Telecom ExperienceDay-to-Day:Insight Global is hiring for a product owner to sit 100% onsite in Stamford, CT for a large, telecommunication company. This person will be joining the Customer Operations organization within the Service Reliability & Outage Management team. This team's focus is quicker outage detection before customers are aware of the outage. When outage is generated, the company will automatically deliver proactive notifications along with estimated repair times via customers preferred method of communication: SMS, auto-call, and email. This Product Owner will be joining a team of approximately 8 individuals responsible for the owning the requirements for digital communication for the three journeys. On a day-to-day basis, this product owner will be gathering/writing requirements, creating process flows & journey maps, attending stakeholder & stand-up meetings, and creating PowerPoint Presentations that will be presented at the executive level on these journeys.