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Jul 10, 2024

Salt Lake City, UT

|

Imaging Technician (Healthcare)

|

Perm

|

$60k - $65k (estimate)

{"JobID":367562,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-111.875818181818,"Longitude":40.7628181818182,"Distance":null},"State":"Utah","Zip":"84111","ReferenceID":"CLT-717693","PostedDate":"\/Date(1720610216000)\/","Description":"An Employer is seeking a Medical Device Associate for a medical device company to sit in the Los Angeles, CA area. Under the guidance of the Director of Operations, and Implementation Project Manager, this Informatics Associate is responsible for the education and training of clinicians (client\u0027s) using the current Anesthesia and Perfusion Quantum Informatics software and other activities related to customer support.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Medical Device Assistant","City":"Salt Lake City","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Experience within a healthcare/medical environment (could be an internship, volunteering experience, or an entry level position -- an example could be maybe a med asst, med tech, Xray tech, radiology tech, worked with doctors or nurses, etc.) -Willingness to travel up to 70% of the time -VERY self-driven personality -Bachelor\u0027s degree","Skills":"-Worked hands on with EMR (Electronic Medical Records) -Experience interacting with customers via phone, email, and in person -Respiratory Therapist or RN experience -Adaptable to different hospital work environments","Industry":"Imaging Technician (Healthcare)","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":65000.0000,"SalaryLow":60000.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

An Employer is seeking a Medical Device Associate for a medical device company to sit in the Los Angeles, CA area. Under the guidance of the Director of Operations, and Implementation Project... Manager, this Informatics Associate is responsible for the education and training of clinicians (client's) using the current Anesthesia and Perfusion Quantum Informatics software and other activities related to customer support.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Jul 10, 2024

Chicago, IL

|

Imaging Technician (Healthcare)

|

Perm

|

$60k - $65k (estimate)

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An Employer is seeking a Medical Device Associate for a medical device company to sit in the Los Angeles, CA area. Under the guidance of the Director of Operations, and Implementation Project... Manager, this Informatics Associate is responsible for the education and training of clinicians (client's) using the current Anesthesia and Perfusion Quantum Informatics software and other activities related to customer support.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Jun 25, 2024

Valencia, CA

|

QA

|

Perm

|

$160k - $200k (estimate)

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A client in the Medical Device space is seeking a Sr. Quality Manager to oversee a team of Senior + Principal Engineers supporting Risk Management, Design Assurance, and Reliability within their... Neuromodulation division. This resource will collaborate across the business to drive compliance and improvement within the Quality System. The Sr. Quality Manager will be responsible for managing Quality efforts across both New Product Development and Sustaining/Post Market Support. The ideal candidate will be well versed in Design Assurance, Design Controls, and Risk Assessment best practices with experience in the Medical Device field. The client is seeking a resource who can not only maintain their current Quality System in compliance with all applicable client + international regulations, but also make suggestions to drive continuous improvement.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Jul 12, 2024

Grand Rapids, MI

|

Engineering (Non IT)

|

Contract

|

$46 - $57 (hourly estimate)

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A large medical device company is looking to grow their Packaging and Labeling team by adding a Sr Design Packaging Engineer to sit onsite in Grand Rapids, MI for a yearlong contract. This person... will have a strong career within the packaging space and experience as an individual contributor on a team. They will support and lead various sustaining packaging engineering projects with focus on quality, cost savings, and service. They will generate and execute packaging remediation/qualification plans for sterile barrier systems and non-sterile medical device packaging. They will define qualification plans, author/execute DV, aging protocols, testing, and closing reports. Additionally this person will utilize quality and regulatory compliance knowledge to support regulatory body audits, CAPA, NCMR and provide innovative ideas to ensure compliance to latest industry practices. This all will contribute to the design and qualification of packaging systems. They will evaluate the current state of various medical device product packaging design; perform gap analysis on existing studies to the latest industry standards such as ISO11607 Part 1 and 2. Lastly, they will determine packaging specifications according to the nature of the product, cost limitations, legal requirements, and the type of device protection required. Then they will update packaging material specifications and technical documentation. The ideal candidate will come from a medical device or pharmaceutical background and comfortable with going onsite 3 days a week to Grand Rapids, MI. This position will pay $52-55/hr.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Jun 25, 2024

Valencia, CA

|

Electrical Engineering

|

Contract

|

$36 - $45 (hourly estimate)

{"JobID":365271,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-118.535818181818,"Longitude":34.4122727272727,"Distance":null},"State":"California","Zip":"91355","ReferenceID":"LAX-714546","PostedDate":"\/Date(1719350058000)\/","Description":"An Insight Global employer is looking for a Firmware Verification engineer to join their embedded software team. This role is for one of our medical device clients and will be dealing with an existing device in the current portfolio of urology products. The ideal candidate will have prior experience in quality within a regulated environment, proficiency with PHP scripting language and local to the greater Los Angeles area. This position has a starting annual compensation of $90,000.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Firmware Verification Engineer","City":"Valencia","ExpirationDate":null,"PriorityOrder":0,"Requirements":"2+ years experience as a verification engineer.Proficiency with PHP scripting language.Bachelor\u0027s degree in computer science or electrical engineering.Prior experience with RF charging.","Skills":"Prior experience in medical device or pharmaceutical industry.","Industry":"Electrical Engineering","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":45.0000,"SalaryLow":36.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

An Insight Global employer is looking for a Firmware Verification engineer to join their embedded software team. This role is for one of our medical device clients and will be dealing with an... existing device in the current portfolio of urology products. The ideal candidate will have prior experience in quality within a regulated environment, proficiency with PHP scripting language and local to the greater Los Angeles area. This position has a starting annual compensation of $90,000.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Jul 08, 2024

Golden Valley, MN

|

Business Analysis

|

Contract

|

$38 - $47 (hourly estimate)

{"JobID":367042,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-93.248,"Longitude":44.9702727272727,"Distance":null},"State":"Minnesota","Zip":"55416","ReferenceID":"MSP-716812","PostedDate":"\/Date(1720440982000)\/","Description":"Insight Global is seeking a Jr Business Analyst to join the team of one of our local medical device clients. In this role, you will be working closely with a Sr BA on the team within the Agile development process. This role involves applying Agile principles, refining user stories, conducting functional reviews, and promoting collaboration within the team. Additionally, tasks in Azure DevOps (ADO) include completing work items, setting up and refining prioritization of backlog PBI/Projects per team\u0027s process requirements. This is a fast-paced role that requires someone with a go-getter mentality and excellent communication skills. This is a hybrid role working onsite in Golden Valley, MN 3x a week. Post training period, the hybrid requirement will become more flexible. This opportunity is seeking to pay between $35-45/hr with flexibility based on experience.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Jr Business Analyst","City":"Golden Valley","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Bachelors degree1-3 years of professional work experience as a BAGo getter personality and mindset, comfortable with autonomyProfessional work experience requirements gathering and meeting with stakeholdersStrong communication skills","Skills":"Quality documentation experienceMicrosoft ADO experience Medical device industry experience","Industry":"Business Analysis","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":47.0000,"SalaryLow":37.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is seeking a Jr Business Analyst to join the team of one of our local medical device clients. In this role, you will be working closely with a Sr BA on the team within the Agile... development process. This role involves applying Agile principles, refining user stories, conducting functional reviews, and promoting collaboration within the team. Additionally, tasks in Azure DevOps (ADO) include completing work items, setting up and refining prioritization of backlog PBI/Projects per team's process requirements. This is a fast-paced role that requires someone with a go-getter mentality and excellent communication skills. This is a hybrid role working onsite in Golden Valley, MN 3x a week. Post training period, the hybrid requirement will become more flexible. This opportunity is seeking to pay between $35-45/hr with flexibility based on experience.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Jul 11, 2024

Irvine, CA

|

QA

|

Contract,Perm Possible

|

$19 - $24 (hourly estimate)

{"JobID":368181,"JobType":["Contract,Perm Possible"],"EmployerID":null,"Location":{"Latitude":-117.703636363636,"Longitude":33.6963636363636,"Distance":null},"State":"California","Zip":"92618","ReferenceID":"SDG-718671","PostedDate":"\/Date(1720721653000)\/","Description":"An employer is looking for a QC Receiving Inspector to join their team in Irvine, CA. The employer is a growing medical device company producing a diabetes management product for patients and QC Receiving Inspector will join their Quality department. The Inspector is primarily responsible for incoming inspection. They will also occasionally perform in-process and final inspections of components, subassemblies and finished good products.Responsibilities: ? Inspect medical device components, subassemblies, and finished goods including plastic components and electronics? Assessing the acceptability of materials and identifying any defects, recommending improvements as per established procedures.? Ability to use measurement equipment such as micrometer, calipers, and rulers? Ensures all Lot History Records (LHRs) and related quality records are complete and accurate? Initiates nonconformance reports for product that does not meet requirements? Performs simple mathematical calculations required to assist with inspections including product testing? Works alongside Manufacturing Operators on a daily basis in support of the production schedule? Works in accordance with quality system procedures.? Other duties as assigned by Supervisor.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"QC Receiving Inspector","City":"Irvine","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? High school diploma, or equivalent ? 1-2 years of Quality Control Inspection experience in the medical device industry? Understanding of sampling plan methods? Ability to read and understand engineering drawings and specifications? Proficiency required with word processing, spreadsheet and document management software? Proficiency required with basic lab tools such as microscopes, calipers, and other inspection tools? Experience in FDA/GMP/ISO environment preferred","Skills":"","Industry":"QA","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":24.0000,"SalaryLow":19.2000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

An employer is looking for a QC Receiving Inspector to join their team in Irvine, CA. The employer is a growing medical device company producing a diabetes management product for patients and QC... Receiving Inspector will join their Quality department. The Inspector is primarily responsible for incoming inspection. They will also occasionally perform in-process and final inspections of components, subassemblies and finished good products.Responsibilities: ? Inspect medical device components, subassemblies, and finished goods including plastic components and electronics? Assessing the acceptability of materials and identifying any defects, recommending improvements as per established procedures.? Ability to use measurement equipment such as micrometer, calipers, and rulers? Ensures all Lot History Records (LHRs) and related quality records are complete and accurate? Initiates nonconformance reports for product that does not meet requirements? Performs simple mathematical calculations required to assist with inspections including product testing? Works alongside Manufacturing Operators on a daily basis in support of the production schedule? Works in accordance with quality system procedures.? Other duties as assigned by Supervisor.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Jun 24, 2024

Grand Rapids, MI

|

Engineering (Non IT)

|

Contract

|

$48 - $60 (hourly estimate)

{"JobID":364734,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-85.6265454545455,"Longitude":42.9844545454545,"Distance":null},"State":"Michigan","Zip":"49507","ReferenceID":"HAR-713850","PostedDate":"\/Date(1719216968000)\/","Description":"A large medical device company is looking to grow their Packaging and Labeling team by adding a Sr Packaging Engineer to sit onsite in Grand Rapids, MI for a yearlong contract. This person will have a strong career within the packaging space and experience as an individual contributor on a team. The team needs someone to come in and take care of the process validation aspect of packaging and labeling. 50% of their day will be spent working cross functionally with various groups at the manufacturing site. This will entail meetings with manufacturing teams, quality teams, the packaging and labeling engineering team, and the maintenance team. The other 50% of their day will be working on planning on projects and execution of these projects. This entails process development and process validation. This person should be experienced with IQ,OQ,PQ validation model, specifically within packaging FFS equipment. The ideal candidate should be coming from a medical device packaging background who also is experienced within process engineering. This person should have the skillset to be a quick learner while manufacturing and have a background in a manufacturing facility. The pay range will be $50-60/hr. The ideal candidate will come from a medical device background or a similar FDA regulated industry.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Sr Validation Packaging Engineer","City":"Grand Rapids","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? Minimum 5 YOE in packaging ? Experience in packaging FFS equipment process development and validation IQ/OQ/PQ? Experience in manufacturing environment, process or manufacturing engineering? Experience with CAPA ? Established and productive individual contributor with strong team and interpersonal skillsEngineering Degree","Skills":"? Advanced education/ degree ? Medical device/ FDA regulated industry experience, general understanding of medical device packaging and labeling requirement? Project management skills? General understanding of Standard requirements; ISO 11607-2, ISO 13485General knowledge of Six sigma methodology and lean manufacturing tools","Industry":"Engineering (Non IT)","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":60.0000,"SalaryLow":48.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A large medical device company is looking to grow their Packaging and Labeling team by adding a Sr Packaging Engineer to sit onsite in Grand Rapids, MI for a yearlong contract. This person will have... a strong career within the packaging space and experience as an individual contributor on a team. The team needs someone to come in and take care of the process validation aspect of packaging and labeling. 50% of their day will be spent working cross functionally with various groups at the manufacturing site. This will entail meetings with manufacturing teams, quality teams, the packaging and labeling engineering team, and the maintenance team. The other 50% of their day will be working on planning on projects and execution of these projects. This entails process development and process validation. This person should be experienced with IQ,OQ,PQ validation model, specifically within packaging FFS equipment. The ideal candidate should be coming from a medical device packaging background who also is experienced within process engineering. This person should have the skillset to be a quick learner while manufacturing and have a background in a manufacturing facility. The pay range will be $50-60/hr. The ideal candidate will come from a medical device background or a similar FDA regulated industry.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Jun 24, 2024

San Diego, CA

|

Electrical Engineering

|

Perm

|

$170k - $200k (estimate)

{"JobID":364789,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-117.186272727273,"Longitude":32.9258181818182,"Distance":null},"State":"California","Zip":"92121","ReferenceID":"SDG-713571","PostedDate":"\/Date(1719227632000)\/","Description":"An employer in the San Diego, CA area is looking for a Senior Staff Electrical Engineer to join the Medical Device Neuromonitoring team for a Full-time, direct hire role. This role will design electronic circuits for intraoperative neuromonitoring used within our surgical and robotic Medical Device products. From a digital and analog perspective: they will design DC to DC converters, amplifiers, analog to digital conversion, digital to analog conversion, filtering, embedded systems. VHDL - program CPLD, or FPGA, understand the process to implement design. Digital logic programming, make timing correct. This person will need to be strong in:Analog and DigitalProgramming VHDL - program CPLD, or FPGANatural when it comes to IEC 60601 / ISO 13485The first 6-8 months will be initial prototype boards, bring up, debugging, lead to launch of product in 2 - 2.5 years.They will also lead system and product-level technical feasibility and risk assessments. Collaborate with other engineering disciplines to develop hardware architecture to meet product functional and performance requirements.Leads development of engineering solutions in a mixed analog/digital environment including amplifiers, FPGAs, and embedded microcontrollers. Develops complex product verification strategy. Leads collaboration with vendors and procurement team to specify, purchase and oversees fabrication of prototypes and pilot runs of Printed circuit assemblies. Administer and implements design changes to bring the product to the regulated medical device market.Performs engineering analysis; conducts testing and data analysis on a variety of problems to ensure product functionality and reliability. Designs, develops, documents, and releases protocol test processes and procedures based on test results.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Senior Staff Electrical Engineer","City":"San Diego","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- BS Degree in Electrical Engineering or Electronics Engineering (or related discipline)- 10+ years of experience designing, developing, and leading embedded systems, analog, digital, mixed signal circuit design for medical devices.- Digital logic programming using Verilog or VHDL. Programming VHDL - program CPLD, or FPGA- Regulations experience with IEC 60601 / ISO 13485- Analog experience: DC to DC converters, amplifiers, analog to digital conversion, digital to analog conversion, filtering, embedded systems. VHDL - program CPLD, or FPGA, understand the process to implement design. Digital logic programming, make timing correct. Debugging experience- Leadership/mentorship experience in a past role- Embedded C, cplusplus experience","Skills":"- Experience with Neuromonitoring/Neuro Electromechanical medical devices - Robotics experience- Firmware experience- Experience Electrical Engineering with Capital Equipment","Industry":"Electrical Engineering","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":200000.0000,"SalaryLow":170000.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

An employer in the San Diego, CA area is looking for a Senior Staff Electrical Engineer to join the Medical Device Neuromonitoring team for a Full-time, direct hire role. This role will design... electronic circuits for intraoperative neuromonitoring used within our surgical and robotic Medical Device products. From a digital and analog perspective: they will design DC to DC converters, amplifiers, analog to digital conversion, digital to analog conversion, filtering, embedded systems. VHDL - program CPLD, or FPGA, understand the process to implement design. Digital logic programming, make timing correct. This person will need to be strong in:Analog and DigitalProgramming VHDL - program CPLD, or FPGANatural when it comes to IEC 60601 / ISO 13485The first 6-8 months will be initial prototype boards, bring up, debugging, lead to launch of product in 2 - 2.5 years.They will also lead system and product-level technical feasibility and risk assessments. Collaborate with other engineering disciplines to develop hardware architecture to meet product functional and performance requirements.Leads development of engineering solutions in a mixed analog/digital environment including amplifiers, FPGAs, and embedded microcontrollers. Develops complex product verification strategy. Leads collaboration with vendors and procurement team to specify, purchase and oversees fabrication of prototypes and pilot runs of Printed circuit assemblies. Administer and implements design changes to bring the product to the regulated medical device market.Performs engineering analysis; conducts testing and data analysis on a variety of problems to ensure product functionality and reliability. Designs, develops, documents, and releases protocol test processes and procedures based on test results.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Jul 11, 2024

Irvine, CA

|

QA

|

Contract-to-perm

|

$24 - $30 (hourly estimate)

{"JobID":368338,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-117.703454545455,"Longitude":33.6709090909091,"Distance":null},"State":"California","Zip":"92618","ReferenceID":"SDG-718718","PostedDate":"\/Date(1720728867000)\/","Description":"An employer is looking for a Complaints Specialist to join their team in Irvine, CA. The employer is a growing medical device company producing a diabetes management product for patients and the Complaints Specialist will join a Quality team. The Complaints Specialist will provide hands-on complaints handling and ensure customer complaints are reviewed and processed in a timely manner. Duties include, but are not limited to, day to day complaint review, investigation, adverse event reporting and complaints trending.Responsibilities:- Reviewing customer service calls (in Salesforce) and opening complaints where needed- Processing open complaints through investigation and closure- Coding complaints (as-reported and as-found) for trending purposes- Determining if a complaint meets the MDR reporting requirements based upon the event- Performs device history reviews for complaint investigations and gathering of additional information, working closely with other departments to complete investigation reports- Evaluates all information from a regulatory and technical perspective to ensure appropriate analysis and investigation- Interacts with the complaint investigation team regarding event information and investigation report status- Participates in investigations and corrective action arising from customer complaints- Ensures timely completion of complaint closures, including completion of investigations and communicates with supervisor and team members to ensure appropriate actions are taken- Analyzes customer complaints trends and identifies potential corrective or preventive actions- Maintains current and complete complaint files and ensures complaint files and records are in compliance with regulatory requirementsWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Complaint Specialist","City":"Irvine","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- Associate or higher degree in a scientific or engineering discipline, mechanical, electrical or software engineering preferred- 2+ years practical experience in medical device complaint handling process- Knowledge in FDA 21 CFR 820 and 21 CFR 803- Experience working in a medical device industry- Experience navigating electronic complaint system (Salesforce is a plus)- Strong communication and organization skills required- Accuracy, attention to detail, and thoroughness- Proficiency required with Microsoft applications- Experience submitting Medical Device Reports is a plus","Skills":"","Industry":"QA","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":30.0000,"SalaryLow":24.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

An employer is looking for a Complaints Specialist to join their team in Irvine, CA. The employer is a growing medical device company producing a diabetes management product for patients and the... Complaints Specialist will join a Quality team. The Complaints Specialist will provide hands-on complaints handling and ensure customer complaints are reviewed and processed in a timely manner. Duties include, but are not limited to, day to day complaint review, investigation, adverse event reporting and complaints trending.Responsibilities:- Reviewing customer service calls (in Salesforce) and opening complaints where needed- Processing open complaints through investigation and closure- Coding complaints (as-reported and as-found) for trending purposes- Determining if a complaint meets the MDR reporting requirements based upon the event- Performs device history reviews for complaint investigations and gathering of additional information, working closely with other departments to complete investigation reports- Evaluates all information from a regulatory and technical perspective to ensure appropriate analysis and investigation- Interacts with the complaint investigation team regarding event information and investigation report status- Participates in investigations and corrective action arising from customer complaints- Ensures timely completion of complaint closures, including completion of investigations and communicates with supervisor and team members to ensure appropriate actions are taken- Analyzes customer complaints trends and identifies potential corrective or preventive actions- Maintains current and complete complaint files and ensures complaint files and records are in compliance with regulatory requirementsWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to [email protected] learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

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