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May 01, 2024

Saint Paul, MN

|

Business Analyst (BA)

|

Contract

|

$48 - $72 (hourly estimate)

{"JobID":354889,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-93.0919090909091,"Longitude":44.967,"Distance":null},"State":"Minnesota","Zip":"55112","ReferenceID":"MSP-701700","PostedDate":"\/Date(1714598191000)\/","Description":"Insight Global is seeking a Business Analyst for one of our largest medical device clients. For this role, you must be local to Minneapolis, MN and willing to work onsite up to 3x a week in Arden Hills. To be successful in this role, you must have experiences and a background supporting field users, operational functions, and service-oriented teams, preferably within the medical device industry. You will play a crucial role in analyzing requirements and needs for field-facing technology solutions, leading solution assessments, RFP processes, and collaborating with project managers, architects, and delivery teams to execute projects successfully. This role sits within their Commercial IT team and is leadership-facing. Strong communication skills, desire to take lead, and collaborate with others is required.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 HR@insightglobal.com.To 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-level Business Analyst","City":"Saint Paul","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Bachelors degree in business administration, Information Technology, or related field.-Proven experience as a Business Analyst, preferably in medical device industry and with commercial technology solutions.-Experience collaborating/interacting with Sales Enablement, Sales Marketing, or field Sales teams. -Strong analytical and problem-solving skills, with the ability to understand complex business processes and systems.-Experience leading solution assessment activities and RFP processes, including vendor evaluation and selection.-Excellent communication and interpersonal skills, with the ability to collaborate effectively with stakeholders at all levels.-Familiarity with agile methodologies and project management practices, with the ability to work closely with project managers and development teams.-Knowledge of field-facing technology solutions, such as CRM systems, mobile applications, and data analytics tools, is highly desirable.-Ability to multitask and prioritize tasks in a fast-paced environment, while maintaining attention to detail and quality of work.","Skills":"-Medical device industry experience.-Knowledge of change management principles-Familiarity with agile methodologies-Familiarity with Commercial operations processes","Industry":"Business Analyst (BA)","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":72.0000,"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)\/"}

Insight Global is seeking a Business Analyst for one of our largest medical device clients. For this role, you must be local to Minneapolis, MN and willing to work onsite up to 3x a week in Arden... Hills. To be successful in this role, you must have experiences and a background supporting field users, operational functions, and service-oriented teams, preferably within the medical device industry. You will play a crucial role in analyzing requirements and needs for field-facing technology solutions, leading solution assessments, RFP processes, and collaborating with project managers, architects, and delivery teams to execute projects successfully. This role sits within their Commercial IT team and is leadership-facing. Strong communication skills, desire to take lead, and collaborate with others is required.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 HR@insightglobal.com.To 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/ .

Apr 18, 2024

Odessa, FL

|

Engineering (Non IT)

|

Perm

|

$62k - $93k (estimate)

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**3 days a week in-office**We are looking for an Applications Engineer for a medical device contract manufacturer. This person will serve as a go-between of Sales and R&D working with field sales... people and their customers to sketch out and prototype product designs and existing product modifications to an existing catalogue of offerings. This person will be responsible for drawings in SolidWorks, creating BOMs (bill of materials) in the ERP system, and releasing engineering documents. This role will communicate heavily with customers and travel on rare occasions (10-15% for critical needs) and collaborate with customers' engineering teams at times.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 HR@insightglobal.com.To 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/ .

Apr 15, 2024

West Chester, PA

|

Data Warehousing

|

Contract,Perm Possible

|

$38 - $58 (hourly estimate)

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A large Medical Device client is seeking an Analyst to join their Strategic Deployment team. This team is responsible for handling all of the customer territory alignments across their Medical... Technology division. This includes analyzing sales/procedural data to better understand and make strategic decisions on where sales territories can be split, re-aligned, or added, to better achieve target sales. On a day-to-day basis, this individual will be utilizing excel and qliksense to upload files, analyze alignment and headcount data, and create reportable visualizations to make key business decisions for the sales organizations. 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 HR@insightglobal.com.To 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/ .

Apr 23, 2024

Springfield, VA

|

Biomedical Engineering

|

Contract-to-perm

|

$40 - $59 (hourly estimate)

{"JobID":352993,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-77.1533636363636,"Longitude":38.7903636363636,"Distance":null},"State":"Virginia","Zip":"22150","ReferenceID":"HDV-699428","PostedDate":"\/Date(1713878075000)\/","Description":"An employer is looking for a team of Biomedical Cybersecurity Specialists to help in a large application and infrastructure resiliency project. The Specialists will be utilizing hardening guides to coordinate and execute controls to reduce attacks in the medical IoT device environment. Other responsibilities include: working with professionals in delivering a robust cybersecurity program, working with clinical operations to coordinate access to the medical devices through a combination of virtual and onsite support to address high/critical vulnerabilities, partnering with application owners to ensure the medical device IT controls are compliant by tracking and reporting of vulnerability remediation activities. This position requires 75% travel within the local market.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 HR@insightglobal.com.To 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":"Lead BioMed Cybersecurity Specialist","City":"Springfield","ExpirationDate":null,"PriorityOrder":0,"Requirements":"5+ years of experience in technology, biomedical engineering, and/or cybersecurity 2+ years of experience with biomedical engineering, BMET, clinical technology (medical devices and systems including EKG, MRI, security cameras, telemedicine, sensor monitoring, remote surgery, etc.)Leadership skills, comfortable taking on administrative tasksTechnical knowledge of healthcare Internet of Things (IoT,) Internet of Medical Things (IoMT,) or clinical technologyExperience in planned maintenance and corrective activities on medical devicesExperience with IT networking, integration, and interoperability of clinical technologiesFamiliar with healthcare modalities, radiologic technology, safety requirements, electrical and mechanical systems, and networking theory.","Skills":"BMET Related certs: RSTI, ACI, HIMSS, ACCE, ISC2, SANS, GIAC","Industry":"Biomedical Engineering","Country":"US","Division":"IGH","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":59.3880,"SalaryLow":39.5920,"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 team of Biomedical Cybersecurity Specialists to help in a large application and infrastructure resiliency project. The Specialists will be utilizing hardening guides to... coordinate and execute controls to reduce attacks in the medical IoT device environment. Other responsibilities include: working with professionals in delivering a robust cybersecurity program, working with clinical operations to coordinate access to the medical devices through a combination of virtual and onsite support to address high/critical vulnerabilities, partnering with application owners to ensure the medical device IT controls are compliant by tracking and reporting of vulnerability remediation activities. This position requires 75% travel within the local market.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 HR@insightglobal.com.To 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/ .

Feb 07, 2024

Dayton, OH

|

QA

|

Perm

|

$58k - $87k (estimate)

{"JobID":337361,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-84.1730909090909,"Longitude":39.7847272727273,"Distance":null},"State":"Ohio","Zip":"45404","ReferenceID":"CIN-680831","PostedDate":"\/Date(1707304599000)\/","Description":"An employer in the Dayton, OH area is seeking a Quality Engineer to sit locally in Dayton. This individual will be working in fast-paced environment where they will be providing quality assurance support to surgical and medical implant development. They will be conducting engineering studies to solve quality problems and provide guidance on how to improve processes and take preventative action. While on this team, there will be a need for this individual to work with cross functional teams to manage projects and be communicating both internally with stakeholders as well as with external stakeholders. 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 HR@insightglobal.com.To 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":"Plant Quality Engineer","City":"Dayton","ExpirationDate":null,"PriorityOrder":0,"Requirements":"1-3 years of experience as a Quality Engineer within a manufacturing environment (Medical Device industry preferred, but Automotive and Aerospace also relevant)Bachelor\u0027s degree in engineering or equivalent years of experienceProven experience with GD\u0026TExperience creating and auditing standard operating procedures/ work instructions. Involvement in any ISO audits (ISO 13485 preferred)Experience managing a quality management system (no specific one required)","Skills":"Medical Device background","Industry":"QA","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":87000.0000,"SalaryLow":58000.0000,"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 Dayton, OH area is seeking a Quality Engineer to sit locally in Dayton. This individual will be working in fast-paced environment where they will be providing quality assurance... support to surgical and medical implant development. They will be conducting engineering studies to solve quality problems and provide guidance on how to improve processes and take preventative action. While on this team, there will be a need for this individual to work with cross functional teams to manage projects and be communicating both internally with stakeholders as well as with external stakeholders. 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 HR@insightglobal.com.To 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/ .

Apr 30, 2024

Valencia, CA

|

QA

|

Contract

|

$37 - $55 (hourly estimate)

{"JobID":354492,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-118.557090909091,"Longitude":34.4280909090909,"Distance":null},"State":"California","Zip":"91355","ReferenceID":"LAX-700399","PostedDate":"\/Date(1714490184000)\/","Description":"A client in the Medical Device industry is seeking a Sr. Software Quality Assurance Engineer to support the full product development life cycle for their commercial implantable pain management device group. The role will entail development, testing, and validation of software + firmware products within a highly regulated medical device environment. This resource will be responsible for maintaining quality standards of their software systems, validating firmware requirements, and adhering to security compliance requirements throughout the product life cycle from requirements gathering through retirement phases. The ideal candidate will be comfortable creating and executing Design Validation Plans, Protocols, and Reports for system level testing and be detailed regarding documentation of user requirements, hazard analysis, risk assessment, etc. This resource will be joining a team of Product Quality Engineers helping support validation activities encompassing User Needs Requirements, Design Requirements, Functional, Architectural, Module Design Details, Code and Design reviews, Unit tests, Integration tests, System level (black box), Structural (white box), Test Automation, Ad-Hoc/Exploratory test activities, Cybersecurity, Usability, and Risk Management, Design FMEAs, and Hazard Analysis. This role is hybrid, onsite 3 days a week in Valencia, CA.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 HR@insightglobal.com.To 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. Software Quality Engineer","City":"Valencia","ExpirationDate":null,"PriorityOrder":0,"Requirements":"BS Degree in Computer Science or Software/Electrical Engineering5+ years of Software Quality experience OR applicable higher education (MS/PhD)3+ years of Software Testing within a Commercial Product teamManual Testing + Documentation experience within a regulated environmentUnderstanding of the SDLC and applicable technologies (csharp, cplusplus, Swift, Node.js, Java/JavaScript, Cloud, Windows, iOS, Android, Python, LabView)Strong organizational and written/verbal communication skills within team environment","Skills":"Medical Device, Highly Regulated Industry, or Neuromodulation/Implantable device experience.Experience with CAPA, Compliant Handling and External Audit, Risk Management (ISO14971), Pre/Post Market Cybersecurity.Experience with Mobile Application development or Bluetooth technologyUnderstanding of HIPAA and GDPR ComplianceASQ Certified Quality Engineer (CQE) or ASQ Certified Software Quality Engineer (CSQE) certs.","Industry":"QA","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":55.2000,"SalaryLow":36.8000,"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 client in the Medical Device industry is seeking a Sr. Software Quality Assurance Engineer to support the full product development life cycle for their commercial implantable pain management device... group. The role will entail development, testing, and validation of software + firmware products within a highly regulated medical device environment. This resource will be responsible for maintaining quality standards of their software systems, validating firmware requirements, and adhering to security compliance requirements throughout the product life cycle from requirements gathering through retirement phases. The ideal candidate will be comfortable creating and executing Design Validation Plans, Protocols, and Reports for system level testing and be detailed regarding documentation of user requirements, hazard analysis, risk assessment, etc. This resource will be joining a team of Product Quality Engineers helping support validation activities encompassing User Needs Requirements, Design Requirements, Functional, Architectural, Module Design Details, Code and Design reviews, Unit tests, Integration tests, System level (black box), Structural (white box), Test Automation, Ad-Hoc/Exploratory test activities, Cybersecurity, Usability, and Risk Management, Design FMEAs, and Hazard Analysis. This role is hybrid, onsite 3 days a week in Valencia, CA.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 HR@insightglobal.com.To 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/ .

May 02, 2024

Maple Grove, MN

|

Engineering (Non IT)

|

Contract,Perm Possible

|

$29 - $43 (hourly estimate)

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Insight Global is seeking a Manufacuring Engineer I to join a leading Medical Device company in the Twin Cities. This candidate will be working alongside the process, R&D and manufacturing teams to... monitor and control yield within the production of the Watchman product, This role will consist of 50% data gathering and interpretation and 50% process 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 HR@insightglobal.com.To 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/ .

May 01, 2024

Minneapolis, MN

|

Biomedical Engineering

|

Perm

|

$192k - $288k (estimate)

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Reporting directly to the CTO of Medical, we are looking for a Director of R&D. This individual will lead a team in the development of products ad processes to ensure device design pass timely and in... budget. Additionally the director of R&D will have global responsibility for the development engineering organization in the medical devices product business unit. The perfect candidate will need a deep understanding of the technologies and manufacturing processes used in the device industry. Overall this director needs to be a leader who is passionate about people leadership, process development and strategic planning and will aspire to grow in their career into VP or executive leadership roles. 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 HR@insightglobal.com.To 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/ .

May 01, 2024

Saint Paul, MN

|

Project Manager

|

Contract

|

$53 - $79 (hourly estimate)

{"JobID":354888,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-93.0914545454545,"Longitude":44.9658181818182,"Distance":null},"State":"Minnesota","Zip":"55112","ReferenceID":"MSP-701699","PostedDate":"\/Date(1714598191000)\/","Description":"Insight Global is seeking a Project Manager for one of our largest medical device clients. For this role, you must be local to Minneapolis, MN and willing to work onsite up to 1-2x a week in Arden Hills. The ideal candidate has strong experience driving projects from scratch, organizing teams, managing communication and stakeholder relationships, and building comprehensive project plans and roadmaps. Additionally, you will be responsible for developing change management plans to ensure successful adoption of project deliverables. The ability to lead teams through solution assessment, RFP processes and vendor selection skills are essential for this role. 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 HR@insightglobal.com.To 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-level Project Manager","City":"Saint Paul","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Bachelor\u0027s degree in business administration, Project Management, or related field.-Ideally 7 years of experience in project management. -Experience working cross-functionally with Sales Enablement, Sales Marketing and Field Sales teams. -Proven experience in project management roles, with a track record of successfully leading initiatives from inception to completion.Strong organizational and leadership skills, with the ability to effectively coordinate teams, manage communication, and build stakeholder relationships.-Excellent communication skills, both verbal and written, with the ability to articulate complex concepts and ideas to diverse audiences.-Proficiency in project management tools and software (e.g., Microsoft Project, Jira) to develop and manage project plans and timelines.-Experience in change management methodologies and techniques, with the ability to develop and implement effective change management plans.-Experience leading teams through solution assessment, RFP processes, and vendor selection is highly desirable.","Skills":"-Medical device or quality regulated-industry experience-PMP certification","Industry":"Project Manager","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":79.2000,"SalaryLow":52.8000,"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 Project Manager for one of our largest medical device clients. For this role, you must be local to Minneapolis, MN and willing to work onsite up to 1-2x a week in Arden... Hills. The ideal candidate has strong experience driving projects from scratch, organizing teams, managing communication and stakeholder relationships, and building comprehensive project plans and roadmaps. Additionally, you will be responsible for developing change management plans to ensure successful adoption of project deliverables. The ability to lead teams through solution assessment, RFP processes and vendor selection skills are essential for this role. 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 HR@insightglobal.com.To 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/ .

Apr 11, 2024

Somerville, NJ

|

Technical Writer

|

Contract

|

$28 - $42 (hourly estimate)

{"JobID":350735,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.6443636363636,"Longitude":40.5454272727273,"Distance":null},"State":"New Jersey","Zip":"08876","ReferenceID":"NNJ-696768","PostedDate":"\/Date(1712837819000)\/","Description":"One of our large pharmaceutical and medical device clients is looking for a doc management specialist strong in technical writing to join a project team. This individual will be responsible for writing quality procedures, following SOPs, assisting in internal \u0026 regulatory audits, and overall management of regulatory healthcare procedural documents. This role will involve conducting research to ensure content is accurate and gathering and organizing information in various functional areas. This role requires an on-site presence in New Brunswick, NJ 4x a week.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 HR@insightglobal.com.To 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":"Document Management Specialist","City":"Somerville","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-5+ years\u0027 experience with technical writing-Experience within pharmaceutical or medical device industries-3+ years\u0027 experience with regulatory document management -Knowledge of internal or regulatory audits-Experience following SOPs-Bachelor\u0027s Degree","Skills":"-Experience utilizing a Quality Management System-Experience supporting LMS programs","Industry":"Technical Writer","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":42.0000,"SalaryLow":28.0000,"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)\/"}

One of our large pharmaceutical and medical device clients is looking for a doc management specialist strong in technical writing to join a project team. This individual will be responsible for... writing quality procedures, following SOPs, assisting in internal & regulatory audits, and overall management of regulatory healthcare procedural documents. This role will involve conducting research to ensure content is accurate and gathering and organizing information in various functional areas. This role requires an on-site presence in New Brunswick, NJ 4x a week.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 HR@insightglobal.com.To 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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