Test Engineer Salary in Connecticut, USA

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.

Test Engineer I - Robotic Surgical Technologies Operating UnitThe Test Engineer shall support test activities to best meet the project's requirements. This position will be a part of a R&D Early Technologies team and will interface with cross-functional team members. You will be responsible for executing tests, analyzing data, documenting results, and ensuring that all documentation passes quality review.Location: North Haven, CTCareers that Change LivesYou will join a team of mechanical, electrical and software engineers responsible for further development and enhancement of the globally launched Medtronic's Robotic Assisted Surgery platform beyond commercial launch and production scale-up: https://www.medtronic.com/surgical/roboticsOperating UnitThe Robotic Surgical Technologies Operating Unit strives to enable earlier diagnosis, better treatment, faster complication-free recovery, and enhanced patient outcomes through less invasive surgical solutions. We 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 Execute and document System tests Author Test Reports and route documents for approval (strong writing skills) Create quality and safety related documentation to support validity of test. Communicate test related activities and results with multi-disciplinary team members Perform gauge repeatability and reproducibility Provide input to engineers to assist in the development of test protocols and prototype builds. Perform mechanical and electrical testing to evaluate new and existing products. Generate and analyze test data, and report results per departmental procedures. Participate in continuous improvement activities of a Testing Services team. May serve as an extended team member for engineering team meetings. Train operators to appropriate SOP's Adhere to safety policies and procedures. Designs, develops, and implements testing methods and equipment. Plans and arranges the labor, schedules, and equipment required for testing and evaluating standard and special devices. Provides test area with parameters for sample testing and specifies tests to be performed. Additional tasks as assigned Must Have: Minimum Requirements Bachelor's Degree with 0 years of engineering experience Nice to Have Bachelor's Degree in a technical discipline, preferably engineering (Biomedical, Mechanical, or Electrical Engineering) with 1 year working in a STEM field. Experience with medical device testing at Medtronic Understanding of creating test methods for verifying product requirements Familiarity with basic statistics and use of Minitab Ability to work with QA to ensure testing meets Quality and Regulatory needs. Ability to work with Systems, Mechanical, Electrical and Software engineers when discovering, documenting, and resolving issues. Experience using oscilloscope, force gauges, and LabVIEW. 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.

This is what you will do: This position is responsible for leading research, design and execute 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. The candidate will support the development of a variety of manufacturing unit operations including, but not limited to, 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, including but not limited to 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, the candidate will support deviation investigations, change controls, and CAPAs utilizing 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 as necessary in-person on-site manufacturing support. This position is expected to interact regularly with cross-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: Lead the design and execute studies for Alexion pharmaceuticals' clinical drug candidates and commercial products, support tech transfer activities for internal manufacturing and contract manufacturing sites Lead progression of projects with cross functional stakeholders, as well as understand the cross functional implication of project activities and decisions with minimal supervision Prioritizing multiple assigned tasks and projects independently and as part of the team Contribute to the development of strategic project plans for molecules in clinical development Author SOPs, study protocols and technical reports with minimal supervision Participate in cross-functional development teams representing Injectable Drug Product Development Maintain 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. Actively participate in department and team meetings including assuming ownership and delivering on assign action items Develop presentations for meetings with internal and external stakeholders with minimal supervision Mentor and train junior Associate Scientists and Engineers regarding drug product development You will need to have: Bachelor's degree in Chemical Engineering, Chemistry, Biochemistry, Pharmaceutical Sciences, or relevant Engineering/Life Sciences field with 7+ years of relevant experience or Master's degree with 6+ years of relevant work experience Self-driven initiative to find resolution for technical challenges Excellent interpersonal, collaborative and communication skills The duties of this role are generally 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 development is preferred Previous experience in biotherapeutics development as well as relevant knowledge of cGMP and Quality expectations for PPQs and BLA is preferred Scientific understanding of protein stability, thermodynamics, mechanism of protein degradation, biotherapeutics drug formulation development and analytical tools used to test formulations is a plus High level proficiency in MS Office software including Word, Excel, Outlook, Visio, and PowerPoint In-person statement for 4 days in the office: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.

Careers that Change Lives Our space, the medical device and healthcare industry, is rapidly changing. It always has been that way. With remote monitoring, wearables, robotics, AR/VR, telemedicine, and much more, agility and responsiveness are key to our success. Experience what it's like to work at a company with an exciting product pipeline full of patented inventions driving innovation in the healthcare space. Operating Unit Our Surgical OU is one new, powerful operating unit bringing together the people and product portfolio of Surgical Innovations and Surgical Robotics. We'll approach the market with a unified approach from concept single strategy, capitalize on our global commercial capabilities, and prove the power of our combined portfolio.With the Medtronic Mission as our North Star, we will build on our legacy of proven surgical solutions and advance the promise of robotics and digital solutions for the benefit of Medtronic and the customers and patients we serve. A Day in the Life As a Test Engineer II, you will be responsible for the end-to-end process involved with demonstrating that our System meets our product requirements.This includes:Designs, develops, and implements testing methods and equipment towards system and sub-system requirements§ Reviewing and providing feedback on product requirements§ Reviewing design descriptions of controls, software, and hardware to understand how System operates with respect to requirements§ Perform Root Cause Analysis by investigating negative test and/or analysis results, including getting hands-on in the lab with the System to troubleshoot test results§ Developing Test Method Validation Protocols, executing Test Method Validation, and writing Test Method Validation Reports§ Analyzing test data using statistical methods§ Collaborating and communicating with cross-functional team members on verification plans, including project management, quality, regulatory, system architecture, design teams, software teams and testing teams§ Provides test area with parameters for sample testing and specifies tests to be performed.Compiles data and defines changes required in testing equipment, testing procedures, manufacturing processes, or new testing requirements.§ Providing guidance and oversight to test and/or analysis methods developed in support of the verification strategy§ Analyzing system and/or subsystem designs and preparing verified-by-design reports§ Determining regression impact from design and/or software changes§ Planning needed testing activities, and participating in SCRUM processes as neededMust Have: Minimum Requirements § Bachelor's degree in Engineering with minimum of 2 years of engineering experience or Advanced degree in Engineering with 0 years of engineering experience Nice to Have § Strong understanding of complex, electro-mechanical, software-controlled devices§ Strong understanding of Systems Engineering principles and tools§ Strong understanding of troubleshooting and root cause analysis§ Demonstrated use of statistical analysis tools commonly used in Engineering, preferably using Minitab.§ Working knowledge of ISO 13485, ISO 14971, 21 CFR 820, IEC 60601-1 and MDD§ Experience with robotics, especially robotic medical devicesAbout 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)

Test Engineer I - Surgical Operating UnitOur Surgical OU is one new, powerful operating unit bringing together the people and product portfolio of Surgical Innovations and Surgical Robotics. We'll approach the market with a unified approach from concept single strategy, capitalize on our global commercial capabilities, and prove the power of our combined portfolio.With the Medtronic Mission as our North Star, we will build on our legacy of proven surgical solutions and advance the promise of robotics and digital solutions for the benefit of Medtronic and the customers and patients we serve.This role is based in North Haven, CT and will not be offering relocation assistance.Careers that Change LivesEngineers are indispensable to achieving our Mission. That's why we empower you to bring the best of your experience to bear on our market-leading portfolio of innovations. Apply your existing skills and develop new ones, with the training, mentorship and the guidance you need to continue to develop your expertise. With roles in specific business units, as well as at the corporate level, you're sure to find an opportunity to make an impact that's right for you. Today, we're partnering across the industry to confront systemic healthcare challenges - this requires bold leadership. If you want a challenging, energizing, rewarding career that changes lives, join us. Help us bring the next generation of life-changing medical technology to patients worldwide.A Day in the Life Drive the continuous improvement activities of a Testing Services team. Balance multiple projects and responsibilities having to do with test lab maintenance, safety, efficiency improvement, and quality enhancement. Author and manage JSAs (Job Safety Analysis), SDS (Safety Data Sheets), and other EHS compliance documents. Monitor and renew the calibration of various electronic, electrical, and mechanical measurement devices. Manage equipment and test material inventory to help with test planning and reordering. Independently execute and document System tests to support System verification. Document tests via test methods and test reports. Route documents for approval (strong writing skills) Perform Gage R&R studies to validate test methods. Perform IQ/OQ to validate test equipment Perform statistical analysis such as: ANOVA, t-test, tolerance interval, normality test, etc. Prepare and operate various lab equipment such as Instron mechanical testers, oscilloscope, force gauges, data loggers, etc. Some travel may be required depending on the project demands at the time. Designs, develops, and implements testing methods and equipment. Plans and arranges the labor, schedules, and equipment required for testing and evaluating standard and special devices. Provides test area with parameters for sample testing and specifies tests to be performed. Compiles data and defines changes required in testing equipment, testing procedures, manufacturing processes, or new testing requirements. Responsible for testing all customer samples and for special tests that cannot be performed in the test area. Additional tasks as assigned Must Have: Minimum Requirements Bachelors degree with 0 years of engineering experience Nice to Have Bachelor's Degree in a technical field such as engineering 1+ year of medical device Test Engineering experience Knowledge and experience with Medtronic's Surgical Operating Unit and products Excellent oral and written communication skills Ability to effectively manage and prioritize multiple tasks and projects in an ambiguous environment Experience with Medical Product verification and FDA guidance. Thorough understanding of creating test methods for verifying product requirements and validating test methods (Gage R&R) Experience creating IQ/OQ/PQ protocols and executing them. Experience with basic statistics and use of Minitab Experience working with QA to ensure testing meets Quality and Regulatory needs. Experience working with Systems, Mechanical, Electrical and Software engineers when discovering,documenting, and resolving issues. Experience using Instron mechanical tester, oscilloscope, force gauges, and LabVIEW 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.

Test Engineer II - Surgical Operating UnitOur Surgical OU is one new, powerful operating unit bringing together the people and product portfolio of Surgical Innovations and Surgical Robotics. We'll approach the market with a unified approach from concept single strategy, capitalize on our global commercial capabilities, and prove the power of our combined portfolio.With the Medtronic Mission as our North Star, we will build on our legacy of proven surgical solutions and advance the promise of robotics and digital solutions for the benefit of Medtronic and the customers and patients we serve.This role is based in North Haven, CT and will not be offering relocation assistance.Careers that Change LivesEngineers are indispensable to achieving our Mission. That's why we empower you to bring the best of your experience to bear on our market-leading portfolio of innovations. Apply your existing skills and develop new ones, with the training, mentorship and the guidance you need to continue to develop your expertise. With roles in specific business units, as well as at the corporate level, you're sure to find an opportunity to make an impact that's right for you. Today, we're partnering across the industry to confront systemic healthcare challenges - this requires bold leadership. If you want a challenging, energizing, rewarding career that changes lives, join us. Help us bring the next generation of life-changing medical technology to patients worldwide.A Day in the Life Drive the continuous improvement activities of a Testing Services team. Balance multiple projects and responsibilities having to do with test lab maintenance, safety, efficiency improvement, and quality enhancement. Author and manage JSAs (Job Safety Analysis), SDS (Safety Data Sheets), and other EHS compliance documents. Monitor and renew the calibration of various electronic, electrical, and mechanical measurement devices. Manage equipment and test material inventory to help with test planning and reordering. Independently execute and document System tests to support System verification. Document tests via test methods and test reports. Route documents for approval (strong writing skills) Perform Gage R&R studies to validate test methods. Perform IQ/OQ to validate test equipment Perform statistical analysis such as: ANOVA, t-test, tolerance interval, normality test, etc. Prepare and operate various lab equipment such as Instron mechanical testers, oscilloscope, force gauges, data loggers, etc. Some travel may be required depending on the project demands at the time. Designs, develops, and implements testing methods and equipment. Plans and arranges the labor, schedules, and equipment required for testing and evaluating standard and special devices. Provides test area with parameters for sample testing and specifies tests to be performed. Compiles data and defines changes required in testing equipment, testing procedures, manufacturing processes, or new testing requirements. Responsible for testing all customer samples and for special tests that cannot be performed in the test area. Additional tasks as assigned Must Have: Minimum Requirements Bachelors degree with 2 years of engineering experience OR An advanced degree with 0 years of engineering experience Nice to Have Bachelor's Degree/Advanced Degree in a technical field such as engineering 2+ years of medical device Test Engineering experience Knowledge and experience with Medtronic's Surgical Operating Unit and products Excellent oral and written communication skills Ability to effectively manage and prioritize multiple tasks and projects in an ambiguous environment Experience with Medical Product verification and FDA guidance. Thorough understanding of creating test methods for verifying product requirements and validating test methods (Gage R&R) Experience creating IQ/OQ/PQ protocols and executing them. Experience with basic statistics and use of Minitab Experience working with QA to ensure testing meets Quality and Regulatory needs. Experience working with Systems, Mechanical, Electrical and Software engineers when discovering,documenting, and resolving issues. Experience using Instron mechanical tester, oscilloscope, force gauges, and LabVIEW 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.

Test Engineer I - Surgical Operating UnitOur Surgical OU is one new, powerful operating unit bringing together the people and product portfolio of Surgical Innovations and Surgical Robotics. We'll approach the market with a unified approach from concept single strategy, capitalize on our global commercial capabilities, and prove the power of our combined portfolio.With the Medtronic Mission as our North Star, we will build on our legacy of proven surgical solutions and advance the promise of robotics and digital solutions for the benefit of Medtronic and the customers and patients we serve.This role is based in North Haven, CT and will not be offering relocation assistance.Careers that Change LivesEngineers are indispensable to achieving our Mission. That's why we empower you to bring the best of your experience to bear on our market-leading portfolio of innovations. Apply your existing skills and develop new ones, with the training, mentorship and the guidance you need to continue to develop your expertise. With roles in specific business units, as well as at the corporate level, you're sure to find an opportunity to make an impact that's right for you. Today, we're partnering across the industry to confront systemic healthcare challenges - this requires bold leadership. If you want a challenging, energizing, rewarding career that changes lives, join us. Help us bring the next generation of life-changing medical technology to patients worldwide.A Day in the Life Drive the continuous improvement activities of a Testing Services team. Balance multiple projects and responsibilities having to do with test lab maintenance, safety, efficiency improvement, and quality enhancement. Author and manage JSAs (Job Safety Analysis), SDS (Safety Data Sheets), and other EHS compliance documents. Monitor and renew the calibration of various electronic, electrical, and mechanical measurement devices. Manage equipment and test material inventory to help with test planning and reordering. Independently execute and document System tests to support System verification. Document tests via test methods and test reports. Route documents for approval (strong writing skills) Perform Gage R&R studies to validate test methods. Perform IQ/OQ to validate test equipment Perform statistical analysis such as: ANOVA, t-test, tolerance interval, normality test, etc. Prepare and operate various lab equipment such as Instron mechanical testers, oscilloscope, force gauges, data loggers, etc. Some travel may be required depending on the project demands at the time. Designs, develops, and implements testing methods and equipment. Plans and arranges the labor, schedules, and equipment required for testing and evaluating standard and special devices. Provides test area with parameters for sample testing and specifies tests to be performed. Compiles data and defines changes required in testing equipment, testing procedures, manufacturing processes, or new testing requirements. Responsible for testing all customer samples and for special tests that cannot be performed in the test area. Additional tasks as assigned Must Have: Minimum Requirements Bachelor's degree with 0 years of engineering experience Nice to Have Bachelor's Degree in a technical field such as engineering 1+ year of medical device Test Engineering experience Knowledge and experience with Medtronic's Surgical Operating Unit and products Excellent oral and written communication skills Ability to effectively manage and prioritize multiple tasks and projects in an ambiguous environment Experience with Medical Product verification and FDA guidance. Thorough understanding of creating test methods for verifying product requirements and validating test methods (Gage R&R) Experience creating IQ/OQ/PQ protocols and executing them. Experience with basic statistics and use of Minitab Experience working with QA to ensure testing meets Quality and Regulatory needs. Experience working with Systems, Mechanical, Electrical and Software engineers when discovering,documenting, and resolving issues. Experience using Instron mechanical tester, oscilloscope, force gauges, and LabVIEW 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.

Job Title : Mechanical Test EngineerLocation: Windsor Locks, Connecticut 06096, USAPosition Type: 12 Months Contract (Possible extension) Pay Rate : $40/hr - $67 hr on w2 with Benefits Education:BachelorsJob Description:Design, implement, and maintain test processes for Space Systems hardware using lean philosophies and techniques.Take a leadership role in driving action in the development, planning & implementation of timely and effective corrective actions for problems during product manufacturing and testing.This can involve testing, data analysis, and interface with all aspects of the engineering department.Duties include the interpretation/analysis of customer test requirements and subsequent cost estimates to support an appropriate test program.Responsibilities also include daily interface with Program, Manufacturing, Quality and Engineering organizations to ensure that customer committed hardware and data deliveries are consistently met.Typical Duties:Support laboratory testing of space hardware.Develop and validate tooling concepts.Author and maintain operation/test procedures.Preparation of standardized operation/test sheetsDefining test rig and facility requirementsParticipation on program Integrated Product Development teamsReview drawings and concepts, and resolve producibility concerns.Experience with advanced instrumentation and data acquisition systems is required.Knowledge of LabVIEW desired.Experience should also include five years working on the testing of complex mechanical systems, testing of complex mechanical systems, testing of components such as, heat exchangers, pumps, fans, & accumulators.Applicant must have the capability of working independently and be self-motivated.Excellent communication skills, written and verbal are required.Ability to proficiently operate common Microsoft Office software products is required.

Job Description:Design, implement, and maintain test processes for Space Systems hardware using lean philosophies and techniques.Take a leadership role in driving action in the development, planning & implementation of timely and effective corrective actions for problems during product manufacturing and testing.This can involve testing, data analysis, and interface with all aspects of the engineering department.Duties include the interpretation/analysis of customer test requirements and subsequent cost estimates to support an appropriate test program.Responsibilities also include daily interface with Program, Manufacturing, Quality and Engineering organizations to ensure that customer committed hardware and data deliveries are consistently met.Typical Duties:Support laboratory testing of space hardware.Develop and validate tooling concepts.Author and maintain operation/test procedures.Preparation of standardized operation/test sheetsDefining test rig and facility requirementsParticipation on program Integrated Product Development teamsReview drawings and concepts, and resolve producibility concerns.Experience with advanced instrumentation and data acquisition systems is required.Knowledge of LabVIEW desired.Experience should also include five years working on the testing of complex mechanical systems, testing of complex mechanical systems, testing of components such as, heat exchangers, pumps, fans, & accumulators.Applicant must have the capability of working independently and be self-motivated.Excellent communication skills, written and verbal are required.Ability to proficiently operate common Microsoft Office software products is required.Education:Bachelors

2 year contract position 2ND SHIFT: 3pm-11:30pm, pay $33.75/hrJOB DESCRIPTIONThe Test Engineer shall support test activities to best meet the project's requirements. This position will be a part of a R&D Systems Engineering team and will interface with cross-functional team members. You will be responsible for executing tests, analyzing data, documenting results, and ensuring that all documentation passes quality review.You will:Execute and document System testsAuthor Test Reports and route documents for approval (strong writing skills)Create quality and safety related documentation to support validity of test.Communicate test related activities and results with multi-disciplinary team membersPerform gauge repeatability and reproducibilityProvide input to engineers to assist in the development of test protocols and prototype builds.Perform mechanical and electrical testing to evaluate new and existing products.Generate and analyze test data, and report results per departmental procedures.Prepare and operate various lab equipment such as Instron mechanical testers, visual inspection, autoclaves, etc.Participate in continuous improvement activities of a Testing Services team.May serve as an extended team member for engineering team meetings.Train operators to appropriate SOP'sAdhere to safety policies and procedures.Must Have:Bachelor's Degree and 0-1 years of relevant experienceNice to have:Bachelor's Degree in a technical discipline, preferably engineering (Biomedical, Mechanical, or Electrical Engineering) with 1 year working in a STEM field. Understanding of creating test methods for verifying product requirementsFamiliarity with basic statistics and use of MinitabAbility to work with QA to ensure testing meets Quality and Regulatory needs.Ability to work with Systems, Mechanical, Electrical and Software engineers when discovering, documenting, and resolving issues.Experience using oscilloscope, force gauges, and LabVIEW