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9 jobs found for manufacturing in seabrook, new hampshire

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    • portsmouth, new hampshire
    • permanent
    • $125,000 - $155,000 per year
    job summary: Our client in the Portsmouth NH area is looking to add a Sr Electrical Engineer to their growing team. Candidates interested should have a minimum of a BSEE and 8 years of relevant experience, preferably in the Medical Device industry. For further information and immediate consideration please apply below and call us today. Thank you.   location: Portsmouth, New Hampshire job type: Permanent salary: $125,000 - 155,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: How you contribute: Responsible for ensuring product engineering is compliant with global medical device design control requirements.Project management for engineering changes or projects where a small project team is required to achieve the project goals.The primary R&D resource assigned to product design projects for the development of electromechanical assemblies, electronics, wired and wireless communication design, as well as electrical safety and EMC related design elements associated with the development of medical devices.Maintains and updates specifications, board design, drawings and other documentation relevant the product as defined by the quality system.The engineer will be responsible for a variety of activities on new product development including design, prototyping, systems integration support, verification and validation, design for manufacture/manufacturing transferMaintains documentation related to materials of concern in support of requirements related to REACH, RoHS, WEEE etc.Assess changes in production and the impact to the design of the product.Write protocols and reports for verification/validation of products throughout their lifecycle.Work closely with software engineering and mechanical engineering team members to integrate design of the systemWill have accountability for design and testing with external labs to support global medical electrical safety and EMC standards (60601 and its associated subparts) #LI-DG2   qualifications: Experience level: ExperiencedMinimum 8 years of experienceEducation: Bachelors (required)  skills: ElectricalElectrical EngineeringElectrical Engineering Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Our client in the Portsmouth NH area is looking to add a Sr Electrical Engineer to their growing team. Candidates interested should have a minimum of a BSEE and 8 years of relevant experience, preferably in the Medical Device industry. For further information and immediate consideration please apply below and call us today. Thank you.   location: Portsmouth, New Hampshire job type: Permanent salary: $125,000 - 155,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: How you contribute: Responsible for ensuring product engineering is compliant with global medical device design control requirements.Project management for engineering changes or projects where a small project team is required to achieve the project goals.The primary R&D resource assigned to product design projects for the development of electromechanical assemblies, electronics, wired and wireless communication design, as well as electrical safety and EMC related design elements associated with the development of medical devices.Maintains and updates specifications, board design, drawings and other documentation relevant the product as defined by the quality system.The engineer will be responsible for a variety of activities on new product development including design, prototyping, systems integration support, verification and validation, design for manufacture/manufacturing transferMaintains documentation related to materials of concern in support of requirements related to REACH, RoHS, WEEE etc.Assess changes in production and the impact to the design of the product.Write protocols and reports for verification/validation of products throughout their lifecycle.Work closely with software engineering and mechanical engineering team members to integrate design of the systemWill have accountability for design and testing with external labs to support global medical electrical safety and EMC standards (60601 and its associated subparts) #LI-DG2   qualifications: Experience level: ExperiencedMinimum 8 years of experienceEducation: Bachelors (required)  skills: ElectricalElectrical EngineeringElectrical Engineering Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • west boxford, massachusetts
    • permanent
    • $75,000 - $90,000 per year
    job summary: Job Summary Responsible for ensuring all aspects of overall product quality within the organization with strong focus on manufacturing support, continuous product/process quality improvement in manufacturing, and management of the QMS. Essential Duties and Responsibilities Provide Quality Engineering support to production and Contract Manufacturers production issuesSupport implementation of 13485:2016 and EU-MDR updates.Support Manufacturing Lean initiatives. Participate/ Lead project teams and attend Gemba board meetings.Chair Laser Defect Reviews with Manufacturing Engineering, Manufacturing, Engineering and QC. Help identify issues, adverse trends and escalate action items.Analyze production data, yields, NCE, for root cause analysis and corrective actionsSupport Quality Management Review by preparing slides as needed, analyzing data,Author, Execute, or Approve Master Validation Plans, Process Validation protocols and reports as necessary.Support/create pFMEAs for product linesRoot cause analysis and implementation of corrective action for process related concerns.Promote QA initiates including establishing, implementing and maintaining the quality management system.Support Supplier Quality initiatives by administrating the SCAR database, issuing SCARs and reviewing actions from suppliers. Help maintain supplier files. Support Supplier Audits as needed.Support QC by authoring, reviewing, approving QC inspection plans for Incoming Inspection. Support Inspection activities as needed when appropriate.Support calibration and preventative maintenance systemSupport internal audits system. Conduct audits, including closing out audit findings, creating audits finding reports and determine proper corrective and preventive actions.Analyze failure, corrective and preventive action to respond to customer complaints, material non-conformity and in process non-conformity.Create and maintain company quality documentation as neededProvide Quality support to new product development projects. Author product quality plans, identity incoming inspection requirements, process validation requirements and source inspection requirements as needed.Update site procedures to ensure compliance with US and international standards.Embody and deliver the "Exceptional Everyday"   location: Westford, Massachusetts job type: Permanent salary: $75,000 - 90,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Job Summary Responsible for ensuring all aspects of overall product quality within the organization with strong focus on manufacturing support, continuous product/process quality improvement in manufacturing, and management of the QMS. Essential Duties and Responsibilities Provide Quality Engineering support to production and Contract Manufacturers production issuesSupport implementation of 13485:2016 and EU-MDR updates.Support Manufacturing Lean initiatives. Participate/ Lead project teams and attend Gemba board meetings.Chair Laser Defect Reviews with Manufacturing Engineering, Manufacturing, Engineering and QC. Help identify issues, adverse trends and escalate action items.Analyze production data, yields, NCE, for root cause analysis and corrective actionsSupport Quality Management Review by preparing slides as needed, analyzing data,Author, Execute, or Approve Master Validation Plans, Process Validation protocols and reports as necessary.Support/create pFMEAs for product linesRoot cause analysis and implementation of corrective action for process related concerns.Promote QA initiates including establishing, implementing and maintaining the quality management system.Support Supplier Quality initiatives by administrating the SCAR database, issuing SCARs and reviewing actions from suppliers. Help maintain supplier files. Support Supplier Audits as needed.Support QC by authoring, reviewing, approving QC inspection plans for Incoming Inspection. Support Inspection activities as needed when appropriate.Support calibration and preventative maintenance systemSupport internal audits system. Conduct audits, including closing out audit findings, creating audits finding reports and determine proper corrective and preventive actions.Analyze failure, corrective and preventive action to respond to customer complaints, material non-conformity and in process non-conformity.Create and maintain company quality documentation as neededProvide Quality support to new product development projects. Author product quality plans, identity incoming inspection requirements, process validation requirements and source inspection requirements as needed.Update site procedures to ensure compliance with US and international standards.Embody and deliver the "Exceptional Everyday"   qualifications: Experience level: ExperiencedMinimum 2 years of experienceEducation: Bachelors  skills: QualityQuality Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information
    job summary: Job Summary Responsible for ensuring all aspects of overall product quality within the organization with strong focus on manufacturing support, continuous product/process quality improvement in manufacturing, and management of the QMS. Essential Duties and Responsibilities Provide Quality Engineering support to production and Contract Manufacturers production issuesSupport implementation of 13485:2016 and EU-MDR updates.Support Manufacturing Lean initiatives. Participate/ Lead project teams and attend Gemba board meetings.Chair Laser Defect Reviews with Manufacturing Engineering, Manufacturing, Engineering and QC. Help identify issues, adverse trends and escalate action items.Analyze production data, yields, NCE, for root cause analysis and corrective actionsSupport Quality Management Review by preparing slides as needed, analyzing data,Author, Execute, or Approve Master Validation Plans, Process Validation protocols and reports as necessary.Support/create pFMEAs for product linesRoot cause analysis and implementation of corrective action for process related concerns.Promote QA initiates including establishing, implementing and maintaining the quality management system.Support Supplier Quality initiatives by administrating the SCAR database, issuing SCARs and reviewing actions from suppliers. Help maintain supplier files. Support Supplier Audits as needed.Support QC by authoring, reviewing, approving QC inspection plans for Incoming Inspection. Support Inspection activities as needed when appropriate.Support calibration and preventative maintenance systemSupport internal audits system. Conduct audits, including closing out audit findings, creating audits finding reports and determine proper corrective and preventive actions.Analyze failure, corrective and preventive action to respond to customer complaints, material non-conformity and in process non-conformity.Create and maintain company quality documentation as neededProvide Quality support to new product development projects. Author product quality plans, identity incoming inspection requirements, process validation requirements and source inspection requirements as needed.Update site procedures to ensure compliance with US and international standards.Embody and deliver the "Exceptional Everyday"   location: Westford, Massachusetts job type: Permanent salary: $75,000 - 90,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Job Summary Responsible for ensuring all aspects of overall product quality within the organization with strong focus on manufacturing support, continuous product/process quality improvement in manufacturing, and management of the QMS. Essential Duties and Responsibilities Provide Quality Engineering support to production and Contract Manufacturers production issuesSupport implementation of 13485:2016 and EU-MDR updates.Support Manufacturing Lean initiatives. Participate/ Lead project teams and attend Gemba board meetings.Chair Laser Defect Reviews with Manufacturing Engineering, Manufacturing, Engineering and QC. Help identify issues, adverse trends and escalate action items.Analyze production data, yields, NCE, for root cause analysis and corrective actionsSupport Quality Management Review by preparing slides as needed, analyzing data,Author, Execute, or Approve Master Validation Plans, Process Validation protocols and reports as necessary.Support/create pFMEAs for product linesRoot cause analysis and implementation of corrective action for process related concerns.Promote QA initiates including establishing, implementing and maintaining the quality management system.Support Supplier Quality initiatives by administrating the SCAR database, issuing SCARs and reviewing actions from suppliers. Help maintain supplier files. Support Supplier Audits as needed.Support QC by authoring, reviewing, approving QC inspection plans for Incoming Inspection. Support Inspection activities as needed when appropriate.Support calibration and preventative maintenance systemSupport internal audits system. Conduct audits, including closing out audit findings, creating audits finding reports and determine proper corrective and preventive actions.Analyze failure, corrective and preventive action to respond to customer complaints, material non-conformity and in process non-conformity.Create and maintain company quality documentation as neededProvide Quality support to new product development projects. Author product quality plans, identity incoming inspection requirements, process validation requirements and source inspection requirements as needed.Update site procedures to ensure compliance with US and international standards.Embody and deliver the "Exceptional Everyday"   qualifications: Experience level: ExperiencedMinimum 2 years of experienceEducation: Bachelors  skills: QualityQuality Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information
    • west boxford, massachusetts
    • permanent
    • $110,000 - $140,000 per year
    job summary: Job Summary Responsible to completely own the radiofrequency product along with new next generation RF products. Qualifications Education Bachelor's degree required Master's degree preferred Specific Area of Study: BSEE/MSEE Experience 8+ years relevant experience Specific Related Experience: Experience in medical device and RF technology Skills Understanding of analog circuitry, power electronics, and RF circuitry at frequencies of 0.1MHz-10MHz, 10W-500WExperience with Schematic capture software, OrCAD CaptureExperience with PCB Layout software, OrCAD PCB EditorRF Class D & E Amplifiers experience, buck, boost transformer drive topologiesExperience developing medical devices in an ISO and FDA regulated environment is preferred.Must be self-motivated, detail oriented, possess strong organizational and communication skills.Works well with others, is thorough and demonstrates good judgment.Takes responsibility for projects, requirements, and schedules.Inspire cooperation and success among the EE team.   location: WESTFORD, Massachusetts job type: Permanent salary: $110,000 - 140,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Author and execute test protocols for the Radiofrequency family of products along with releasing these documents into our SAP PLM system.Improve existing products, providing technical assistance to engineering, manufacturing, and field support.Author technical documents to verify operation of systems design and product support of systems, sub-assemblies and circuit boardsWrite and release ECO'sResponsible for the component selection, electrical modifications and design verification at the PCB and system level.Work cross functionality with Ops and Service on day-to-day needsEmbody and deliver the "Exceptional Everyday"   qualifications: Experience level: ExperiencedMinimum 8 years of experienceEducation: Bachelors (required)  skills: RF DesignCircuit Board DesignComponent Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Job Summary Responsible to completely own the radiofrequency product along with new next generation RF products. Qualifications Education Bachelor's degree required Master's degree preferred Specific Area of Study: BSEE/MSEE Experience 8+ years relevant experience Specific Related Experience: Experience in medical device and RF technology Skills Understanding of analog circuitry, power electronics, and RF circuitry at frequencies of 0.1MHz-10MHz, 10W-500WExperience with Schematic capture software, OrCAD CaptureExperience with PCB Layout software, OrCAD PCB EditorRF Class D & E Amplifiers experience, buck, boost transformer drive topologiesExperience developing medical devices in an ISO and FDA regulated environment is preferred.Must be self-motivated, detail oriented, possess strong organizational and communication skills.Works well with others, is thorough and demonstrates good judgment.Takes responsibility for projects, requirements, and schedules.Inspire cooperation and success among the EE team.   location: WESTFORD, Massachusetts job type: Permanent salary: $110,000 - 140,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Author and execute test protocols for the Radiofrequency family of products along with releasing these documents into our SAP PLM system.Improve existing products, providing technical assistance to engineering, manufacturing, and field support.Author technical documents to verify operation of systems design and product support of systems, sub-assemblies and circuit boardsWrite and release ECO'sResponsible for the component selection, electrical modifications and design verification at the PCB and system level.Work cross functionality with Ops and Service on day-to-day needsEmbody and deliver the "Exceptional Everyday"   qualifications: Experience level: ExperiencedMinimum 8 years of experienceEducation: Bachelors (required)  skills: RF DesignCircuit Board DesignComponent Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • portsmouth, new hampshire
    • permanent
    • $85,000 - $95,000 per year
    job summary: Our client in the greater Portsmouth NH area is looking to add an experienced Hardware Engineer to their growing PLM team. You will be responsible for responsible for various hardware and electrical activities including the ongoing improvement and maintenance of existing product lines. Candidates interested should have a BSEE and a minimum of 3 years relevant experience. For further detail and immediate consideration please apply below and call us today. Thank you.   location: Portsmouth, New Hampshire job type: Permanent salary: $85,000 - 95,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: How you contribute: Assist in managing product life cycle of existing product linesManage Hardware design processes to ensure timely delivery of design and integration into the production of electrical and PCB designsAid in test strategies and executing of design verificationAid in creation of Product and Development Documentation in compliance with Laborie QMS, ISO, and other standardsDesign, implement, and deliver product changes to support sales, marketing, production, and serviceCollaborate with new product development, manufacturing engineering, and quality engineering staff to ensure compliance of new or modified products and processes to company design control and quality system requirementsProvide technical support to regulatory affairs, customer care and marketing staff for product support issues and country registration processesWork with management and development teams to establish best practicesSupport collection and documentation of user's requirements, development plans, time estimates, and resource management #LI-CA1   qualifications: Experience level: ExperiencedMinimum 3 years of experienceEducation: Bachelors (required)  skills: ElectronicsPCB Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Our client in the greater Portsmouth NH area is looking to add an experienced Hardware Engineer to their growing PLM team. You will be responsible for responsible for various hardware and electrical activities including the ongoing improvement and maintenance of existing product lines. Candidates interested should have a BSEE and a minimum of 3 years relevant experience. For further detail and immediate consideration please apply below and call us today. Thank you.   location: Portsmouth, New Hampshire job type: Permanent salary: $85,000 - 95,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: How you contribute: Assist in managing product life cycle of existing product linesManage Hardware design processes to ensure timely delivery of design and integration into the production of electrical and PCB designsAid in test strategies and executing of design verificationAid in creation of Product and Development Documentation in compliance with Laborie QMS, ISO, and other standardsDesign, implement, and deliver product changes to support sales, marketing, production, and serviceCollaborate with new product development, manufacturing engineering, and quality engineering staff to ensure compliance of new or modified products and processes to company design control and quality system requirementsProvide technical support to regulatory affairs, customer care and marketing staff for product support issues and country registration processesWork with management and development teams to establish best practicesSupport collection and documentation of user's requirements, development plans, time estimates, and resource management #LI-CA1   qualifications: Experience level: ExperiencedMinimum 3 years of experienceEducation: Bachelors (required)  skills: ElectronicsPCB Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • andover, massachusetts
    • contract
    • $38 - $43 per hour
    job summary: Job Description In this role, you have the opportunity to Support New Product Development projects within Image Guide Therapy with respect to software, firmware, and hardware from a software design quality assurance perspective. You are responsible for - Leading the creation and review of risk management file to include the risk management plan, product hazard analysis, FMEAs, Software Risk Assessment, Risk Management Matrix, and Benefit Risk Determination. - Ensuring Risk Management is effective utilizing feedback from validation, field service, post market surveillance, manufacturing indicators, CAPAs, HHAs, etc. Expertise in ISO 14971, Risk Management for medical devices and IEC 62304 Medical Device Software. - Support in the creation and review of all medical device software documentation including cyber security assessments such as Data Protection, Privacy, and Security Assessments etc. - Understanding of all aspects of the QMS related to Design Controls. 21 CFR 820, ISO 13485 - Development and status reporting of Quality and Reliability metric during phase reviews. - Participate in Design Verification Planning, Protocol Review, Report Review. - Participate in Design Validation Planning, Protocol Review, Report Review. - Participate in Process Validation Planning, Protocol Review, Report Review. - Provide Guidance on Quality aspects of PDLM Deliverables in addition to Design Verification/Validation. To succeed in this role, you should have the following skills and experience - Electrical, Computer/Software, or Biomedical Engineering degree. - 3+ years of software quality or electrical engineering experience. - ASQ-CQE preferred. - Expertise in applying IEC 60601 and working knowledge with IEC 62304 and other relevant medical device standards - Knowledge in electrical and electronic manufacturing processes - Experience with software development lifecycle mythologies including Agile and SAFe - Familiar with software tools: - Defect tracking and management tools such a Jira or Clearquest. - Statistical software solutions such as JMP or Minitab - Design for reliability concepts and relating complaint history to reliability goals on new projects - strong leadership skills and ability to work in a team environment - Highly motivated hands-on engineer with a proven record of meeting timelines and goals - Must possess strong analytical & problem-solving skills - Non-Product Software Validation, IQ OQ PQ - Non-conforming product investigation, issue and defect tracking, CAPA - Post Market Surveillance and complaint review - Job Posting Description In this role, you have the opportunity to Support New Product Development projects within Image Guide Therapy with respect to software, firmware, and hardware from a design quality assurance perspective. You are responsible for - Lead and support the creation and review of risk management file to include the risk management plan, product hazard analysis, FMEAs, Software Risk Assessment, Risk Management Matrix, and Benefit Risk Determination. - Ensuring Risk Management is effective utilizing feedback from validation, field service, post market surveillance, manufacturing indicators, CAPAs, HHAs, etc. Expertise in ISO 14971, Risk Management for medical devices and IEC 62304 Medical Device Software. - Support in the creation and review of all medical device documentation including cyber security assessments such as Data Protection, Privacy, and Security Assessments etc. - Understanding of all aspects of the QMS related to Design Controls. 21 CFR 820, ISO 13485 - Development and status reporting of Quality and Reliability metric during phase reviews. - Participate in Design Verification Planning, Protocol Review, Report Review. - Participate in Design Validation Planning, Protocol Review, Report Review. - Participate in Process Validation Planning, Protocol Review, Report Review. - Provide Guidance on Quality aspects of PDLM Deliverables in addition to Design Verification/Validation. You are a part of Our solutions combine navigational tools such as catheters and guide wires with advanced software to help confirm the optimal treatment at the point of care: measurement technology, procedure-specific application support and on-board imaging and monitoring with improved anatomical and functional information to optimize therapy delivery. The IGT Devices organization consists of three segments: Coronary, Peripheral Vascular and Electrophysiology. To succeed in this role, you should have the following skills and experience - US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa. - Engineering or related Science degree. - 3+ years of quality engineering experience. - ASQ-CQE preferred. - Graduate degree in Engineering/Science preferred. - Expertise in applying ISO 13485, ISO 14971, IEC 60601 and working knowledge with IEC 62304 and other relevant medical device standards. - Knowledge in manufacturing processes - Experience with medical device development lifecycle mythologies including Agile and SAFe preferred. - Familiar with systems engineering tools including software tools such as, design traceability, defect tracking and management tools such a Jira or Clearquest. - Statistical software solutions such as JMP or Minitab - Design for reliability concepts and relating complaint history to reliability goals on new projects - strong leadership skills and ability to work in a team environment - Highly motivated hands-on engineer/scientist with a proven record of meeting timelines and goals - Must possess strong analytical & problem-solving skills - Knowledge of Non-Product Software Validation, IQ OQ PQ  location: ANDOVER, Massachusetts job type: Contract salary: $38 - 43 per hour work hours: 8am to 4pm education: Bachelors   responsibilities: Leading the creation and review of risk management file to include the risk management plan, product hazard analysis, FMEAs, Software Risk Assessment, Risk Management Matrix, and Benefit Risk Determination. - Ensuring Risk Management is effective utilizing feedback from validation, field service, post market surveillance, manufacturing indicators, CAPAs, HHAs, etc. Expertise in ISO 14971, Risk Management for medical devices and IEC 62304 Medical Device Software. - Support in the creation and review of all medical device software documentation including cyber security assessments such as Data Protection, Privacy, and Security Assessments etc. - Understanding of all aspects of the QMS related to Design Controls. 21 CFR 820, ISO 13485 - Development and status reporting of Quality and Reliability metric during phase reviews. - Participate in Design Verification Planning, Protocol Review, Report Review. - Participate in Design Validation Planning, Protocol Review, Report Review. - Participate in Process Validation Planning, Protocol Review, Report Review. - Provide Guidance on Quality aspects of PDLM Deliverables in addition to Design Verification/Validation.   qualifications: Experience level: Minimum 3 years of experienceEducation: Bachelors (required)  skills: Manual QA Testing (2 years of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information
    job summary: Job Description In this role, you have the opportunity to Support New Product Development projects within Image Guide Therapy with respect to software, firmware, and hardware from a software design quality assurance perspective. You are responsible for - Leading the creation and review of risk management file to include the risk management plan, product hazard analysis, FMEAs, Software Risk Assessment, Risk Management Matrix, and Benefit Risk Determination. - Ensuring Risk Management is effective utilizing feedback from validation, field service, post market surveillance, manufacturing indicators, CAPAs, HHAs, etc. Expertise in ISO 14971, Risk Management for medical devices and IEC 62304 Medical Device Software. - Support in the creation and review of all medical device software documentation including cyber security assessments such as Data Protection, Privacy, and Security Assessments etc. - Understanding of all aspects of the QMS related to Design Controls. 21 CFR 820, ISO 13485 - Development and status reporting of Quality and Reliability metric during phase reviews. - Participate in Design Verification Planning, Protocol Review, Report Review. - Participate in Design Validation Planning, Protocol Review, Report Review. - Participate in Process Validation Planning, Protocol Review, Report Review. - Provide Guidance on Quality aspects of PDLM Deliverables in addition to Design Verification/Validation. To succeed in this role, you should have the following skills and experience - Electrical, Computer/Software, or Biomedical Engineering degree. - 3+ years of software quality or electrical engineering experience. - ASQ-CQE preferred. - Expertise in applying IEC 60601 and working knowledge with IEC 62304 and other relevant medical device standards - Knowledge in electrical and electronic manufacturing processes - Experience with software development lifecycle mythologies including Agile and SAFe - Familiar with software tools: - Defect tracking and management tools such a Jira or Clearquest. - Statistical software solutions such as JMP or Minitab - Design for reliability concepts and relating complaint history to reliability goals on new projects - strong leadership skills and ability to work in a team environment - Highly motivated hands-on engineer with a proven record of meeting timelines and goals - Must possess strong analytical & problem-solving skills - Non-Product Software Validation, IQ OQ PQ - Non-conforming product investigation, issue and defect tracking, CAPA - Post Market Surveillance and complaint review - Job Posting Description In this role, you have the opportunity to Support New Product Development projects within Image Guide Therapy with respect to software, firmware, and hardware from a design quality assurance perspective. You are responsible for - Lead and support the creation and review of risk management file to include the risk management plan, product hazard analysis, FMEAs, Software Risk Assessment, Risk Management Matrix, and Benefit Risk Determination. - Ensuring Risk Management is effective utilizing feedback from validation, field service, post market surveillance, manufacturing indicators, CAPAs, HHAs, etc. Expertise in ISO 14971, Risk Management for medical devices and IEC 62304 Medical Device Software. - Support in the creation and review of all medical device documentation including cyber security assessments such as Data Protection, Privacy, and Security Assessments etc. - Understanding of all aspects of the QMS related to Design Controls. 21 CFR 820, ISO 13485 - Development and status reporting of Quality and Reliability metric during phase reviews. - Participate in Design Verification Planning, Protocol Review, Report Review. - Participate in Design Validation Planning, Protocol Review, Report Review. - Participate in Process Validation Planning, Protocol Review, Report Review. - Provide Guidance on Quality aspects of PDLM Deliverables in addition to Design Verification/Validation. You are a part of Our solutions combine navigational tools such as catheters and guide wires with advanced software to help confirm the optimal treatment at the point of care: measurement technology, procedure-specific application support and on-board imaging and monitoring with improved anatomical and functional information to optimize therapy delivery. The IGT Devices organization consists of three segments: Coronary, Peripheral Vascular and Electrophysiology. To succeed in this role, you should have the following skills and experience - US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa. - Engineering or related Science degree. - 3+ years of quality engineering experience. - ASQ-CQE preferred. - Graduate degree in Engineering/Science preferred. - Expertise in applying ISO 13485, ISO 14971, IEC 60601 and working knowledge with IEC 62304 and other relevant medical device standards. - Knowledge in manufacturing processes - Experience with medical device development lifecycle mythologies including Agile and SAFe preferred. - Familiar with systems engineering tools including software tools such as, design traceability, defect tracking and management tools such a Jira or Clearquest. - Statistical software solutions such as JMP or Minitab - Design for reliability concepts and relating complaint history to reliability goals on new projects - strong leadership skills and ability to work in a team environment - Highly motivated hands-on engineer/scientist with a proven record of meeting timelines and goals - Must possess strong analytical & problem-solving skills - Knowledge of Non-Product Software Validation, IQ OQ PQ  location: ANDOVER, Massachusetts job type: Contract salary: $38 - 43 per hour work hours: 8am to 4pm education: Bachelors   responsibilities: Leading the creation and review of risk management file to include the risk management plan, product hazard analysis, FMEAs, Software Risk Assessment, Risk Management Matrix, and Benefit Risk Determination. - Ensuring Risk Management is effective utilizing feedback from validation, field service, post market surveillance, manufacturing indicators, CAPAs, HHAs, etc. Expertise in ISO 14971, Risk Management for medical devices and IEC 62304 Medical Device Software. - Support in the creation and review of all medical device software documentation including cyber security assessments such as Data Protection, Privacy, and Security Assessments etc. - Understanding of all aspects of the QMS related to Design Controls. 21 CFR 820, ISO 13485 - Development and status reporting of Quality and Reliability metric during phase reviews. - Participate in Design Verification Planning, Protocol Review, Report Review. - Participate in Design Validation Planning, Protocol Review, Report Review. - Participate in Process Validation Planning, Protocol Review, Report Review. - Provide Guidance on Quality aspects of PDLM Deliverables in addition to Design Verification/Validation.   qualifications: Experience level: Minimum 3 years of experienceEducation: Bachelors (required)  skills: Manual QA Testing (2 years of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information
    • west boxford, massachusetts
    • permanent
    • $150,000 - $175,000 per year
    job summary: Job Summary The Director of Systems engineering is responsible for the overall direction, budget and strategy for the Systems Engineering Team with respect to people, process, engineering content and design tools. The Director and their team own the system level design, requirements, reliability and test engineering for capital equipment and associated disposable medical devices. The Director will build on extensive hands-on experience in capital systems development and a deep understanding of technical, end user and patient needs to ensure that systems designs and associated requirements drive project teams to achieve best-in-class medical products. This role is a key leadership position in the R&D team and will strive to recruit and retain a highly capable, collaborative and diverse team of systems engineers. The Systems Team will interact with all areas of the business to ensure timely development of new products and exceptional support of existing designs. Qualifications Education Bachelor's degree required Master's degree preferred Specific Area of Study: B.S. in Electrical, Biomedical, Computer Science or related engineering discipline. Experience 12+ years relevant experience Specific Related Experience: Systems engineering in product development, new product introduction and on-market product support. Skills Passion for delivering best-in-class products to market that exceed customer expectationsstrong leadership skills to both develop and grow a systems team as well as represent their work to the broader organizationMastery of the product development process, design controls, requirements and test (V&V)Core competency in RF and/or optomechanical system design and testBroad experience in capital systems design with a track record of successful product launch5+ yrs experience in a regulated field such as medical device or aerospace/defenseKnowledge of global medical design standards (FDA, ISO, Int'l)Working knowledge of project management, requirements management, board layout and mechanical design software.   location: WESTFORD, Massachusetts job type: Permanent salary: $150,000 - 175,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Overall leadership of the Systems Engineering Team to ensure on-time, on-budget delivery of project objectives with representation to the R&D Leadership Team for the Systems functionStaffing and people leadership of the Systems team to ensure consistent capability, capacity and growth of the people and their domain expertise and executionWorking closely with cross-functional project teams, ensure consistent delivery of Systems activities across system design, requirements definition/management, risk management, test (V&V) and reliabilityWork across commercial, technical and regulatory functions to ensure comprehensive understanding of customer/patient/technology/business needs and clear translation into system requirementsSupport key process deliverables including User Needs Document, Product Requirement spec, traceability, system architecture, FMEA, system verification and validation, and ongoing technical support to operations and serviceCollaborative and hands-on support of project deliverables for quality, regulatory and sustaining to ensure business continuityEducate and mentor the R&D and broader organization on systems engineering best practiceMonitor and ensure both compliance with and documentation of compliance with policies and procedures as outlined in various Company policies, including the Global Approval Authority Matrix and other mandatory policies pursuant to one's job description.Embody and deliver the "Exceptional Everyday"   qualifications: Experience level: ExperiencedMinimum 10 years of experienceEducation: Bachelors (required)  skills: Electrical EngineeringRF Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Job Summary The Director of Systems engineering is responsible for the overall direction, budget and strategy for the Systems Engineering Team with respect to people, process, engineering content and design tools. The Director and their team own the system level design, requirements, reliability and test engineering for capital equipment and associated disposable medical devices. The Director will build on extensive hands-on experience in capital systems development and a deep understanding of technical, end user and patient needs to ensure that systems designs and associated requirements drive project teams to achieve best-in-class medical products. This role is a key leadership position in the R&D team and will strive to recruit and retain a highly capable, collaborative and diverse team of systems engineers. The Systems Team will interact with all areas of the business to ensure timely development of new products and exceptional support of existing designs. Qualifications Education Bachelor's degree required Master's degree preferred Specific Area of Study: B.S. in Electrical, Biomedical, Computer Science or related engineering discipline. Experience 12+ years relevant experience Specific Related Experience: Systems engineering in product development, new product introduction and on-market product support. Skills Passion for delivering best-in-class products to market that exceed customer expectationsstrong leadership skills to both develop and grow a systems team as well as represent their work to the broader organizationMastery of the product development process, design controls, requirements and test (V&V)Core competency in RF and/or optomechanical system design and testBroad experience in capital systems design with a track record of successful product launch5+ yrs experience in a regulated field such as medical device or aerospace/defenseKnowledge of global medical design standards (FDA, ISO, Int'l)Working knowledge of project management, requirements management, board layout and mechanical design software.   location: WESTFORD, Massachusetts job type: Permanent salary: $150,000 - 175,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Overall leadership of the Systems Engineering Team to ensure on-time, on-budget delivery of project objectives with representation to the R&D Leadership Team for the Systems functionStaffing and people leadership of the Systems team to ensure consistent capability, capacity and growth of the people and their domain expertise and executionWorking closely with cross-functional project teams, ensure consistent delivery of Systems activities across system design, requirements definition/management, risk management, test (V&V) and reliabilityWork across commercial, technical and regulatory functions to ensure comprehensive understanding of customer/patient/technology/business needs and clear translation into system requirementsSupport key process deliverables including User Needs Document, Product Requirement spec, traceability, system architecture, FMEA, system verification and validation, and ongoing technical support to operations and serviceCollaborative and hands-on support of project deliverables for quality, regulatory and sustaining to ensure business continuityEducate and mentor the R&D and broader organization on systems engineering best practiceMonitor and ensure both compliance with and documentation of compliance with policies and procedures as outlined in various Company policies, including the Global Approval Authority Matrix and other mandatory policies pursuant to one's job description.Embody and deliver the "Exceptional Everyday"   qualifications: Experience level: ExperiencedMinimum 10 years of experienceEducation: Bachelors (required)  skills: Electrical EngineeringRF Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • beverly, massachusetts
    • permanent
    • $50,000 - $55,000 per year
    job summary: Our client in the Beverly MA area is looking to add two (2) entry level Inside Sales Engineers to their growing team. Candidates with a BS in Mechanical or Chemical Engineering and 1 year of experience are desired. Past Customer Service experience a plus. If you are interested in learning more please apply below and call us today for immediate consideration. Thank you.   location: Beverly, Massachusetts job type: Permanent salary: $50,000 - 55,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Your main responsibilities: - Support District Sales Managers, affiliated representative companies, and end customers through technical application assessment, product presentations and recommendations, quotation generation and periodic contact. - Communicate effectively and efficiently with contacts both internal and external to KROHNE. - Assist affiliated representative companies with product selection and pricing. - Coordinate customer development efforts closely with outside sales representatives and District Sales Managers. - Prepare and follow up on quotations and offers. - Work with resources within company to develop and coordinate technical responses to Requests for Quotation. - Project a positive attitude at all times when working with internal and external customers.   qualifications: Experience level: Entry LevelMinimum 1 year of experienceEducation: Bachelors (required)  skills: Technical SupportMechanical Engineering Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Our client in the Beverly MA area is looking to add two (2) entry level Inside Sales Engineers to their growing team. Candidates with a BS in Mechanical or Chemical Engineering and 1 year of experience are desired. Past Customer Service experience a plus. If you are interested in learning more please apply below and call us today for immediate consideration. Thank you.   location: Beverly, Massachusetts job type: Permanent salary: $50,000 - 55,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Your main responsibilities: - Support District Sales Managers, affiliated representative companies, and end customers through technical application assessment, product presentations and recommendations, quotation generation and periodic contact. - Communicate effectively and efficiently with contacts both internal and external to KROHNE. - Assist affiliated representative companies with product selection and pricing. - Coordinate customer development efforts closely with outside sales representatives and District Sales Managers. - Prepare and follow up on quotations and offers. - Work with resources within company to develop and coordinate technical responses to Requests for Quotation. - Project a positive attitude at all times when working with internal and external customers.   qualifications: Experience level: Entry LevelMinimum 1 year of experienceEducation: Bachelors (required)  skills: Technical SupportMechanical Engineering Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • west boxford, massachusetts
    • permanent
    • $125,000 - $140,000 per year
    job summary: Essential Duties and Responsibilities Contribute to the architecture and implementation of a distributed control system.Conduct and participate in software analysis, planning, design, implementation, and code reviews.Document requirements, architecture, and detailed design specifications.Develop and test high quality software using best practice methodologies.Comfortable with reviewing and offering constructive criticism of board schematics.Collaborate within a multi-disciplinary team (optics, electronics, mechanical) to achieve company goals.Assure software systems meet FDA 510k, EN 62304, and other approval standards as required.Utilize Microsoft Visual Studio 2019+ and Team Foundation Server (TFS) to create and maintain source code, bug reports and requirements.Embody and deliver the "Exceptional Everyday" Qualifications Education ?Bachelor's degree required - BSCS/BSEE Experience ?8+ years relevant experience in embedded software, medical software development experience (FDA 510K, EN62304) required Skills Expert in C/C++ for embedded processorsTest Driven Development (TDD)Agile software development processesHardware/software interfacesRTOS-based architecture and designARM Cortex A9, Microchip PIC processor experience a plusMedical software development experience (FDA 510k, EN62304)Realtime multitasking kernels - QNX, SMX, VxWorks, Integrity, or similar a plus.Windows C#, Embedded Linux, Python experience a plus.Device driver experience a plus.Familiar with unit test philosophy on embedded software   location: Westford, Massachusetts job type: Permanent salary: $125,000 - 140,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Responsible to architect, implement and validate a distributed control architecture that can be applied across multiple hardware platforms. Contribute to the architecture, design, development and troubleshooting of complex real time embedded software and related hardware systems. Work at the interface of hardware and software implementing both control and monitoring algorithms. This includes all aspects from user interfaces to direct hardware control, inter-processor communications and web-based connectivity.   qualifications: Experience level: ExperiencedMinimum 5 years of experienceEducation: Bachelors (required)  skills: Embedded (6 years of experience is required)Arm CortexRTOSC/C++ Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information
    job summary: Essential Duties and Responsibilities Contribute to the architecture and implementation of a distributed control system.Conduct and participate in software analysis, planning, design, implementation, and code reviews.Document requirements, architecture, and detailed design specifications.Develop and test high quality software using best practice methodologies.Comfortable with reviewing and offering constructive criticism of board schematics.Collaborate within a multi-disciplinary team (optics, electronics, mechanical) to achieve company goals.Assure software systems meet FDA 510k, EN 62304, and other approval standards as required.Utilize Microsoft Visual Studio 2019+ and Team Foundation Server (TFS) to create and maintain source code, bug reports and requirements.Embody and deliver the "Exceptional Everyday" Qualifications Education ?Bachelor's degree required - BSCS/BSEE Experience ?8+ years relevant experience in embedded software, medical software development experience (FDA 510K, EN62304) required Skills Expert in C/C++ for embedded processorsTest Driven Development (TDD)Agile software development processesHardware/software interfacesRTOS-based architecture and designARM Cortex A9, Microchip PIC processor experience a plusMedical software development experience (FDA 510k, EN62304)Realtime multitasking kernels - QNX, SMX, VxWorks, Integrity, or similar a plus.Windows C#, Embedded Linux, Python experience a plus.Device driver experience a plus.Familiar with unit test philosophy on embedded software   location: Westford, Massachusetts job type: Permanent salary: $125,000 - 140,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Responsible to architect, implement and validate a distributed control architecture that can be applied across multiple hardware platforms. Contribute to the architecture, design, development and troubleshooting of complex real time embedded software and related hardware systems. Work at the interface of hardware and software implementing both control and monitoring algorithms. This includes all aspects from user interfaces to direct hardware control, inter-processor communications and web-based connectivity.   qualifications: Experience level: ExperiencedMinimum 5 years of experienceEducation: Bachelors (required)  skills: Embedded (6 years of experience is required)Arm CortexRTOSC/C++ Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information
    • newburyport, massachusetts
    • permanent
    • $110,000 - $125,000 per year
    job summary: Our client in the Newburyport MA area is looking to add an experienced Facilities Engineer to their growing team. Candidates interested should have a minimum of 3 years experience and have electrical controls experience. For further detail and immediate consideration please apply below and call us today. Thank you.   location: NEWBURYPORT, Massachusetts job type: Permanent salary: $110,000 - 125,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Essential Duties and Responsibilities Ensure that building and grounds are maintained in accordance with relevant regulations and fiscal considerations.Evaluate short and long-term needs in relation to major facility projects and property improvements including coordination of contractors.Plan, execute and monitor all facility and property improvement projectsCoordinate, arrange, and supervise the completion of corrective and preventive maintenance actions in accordance with operational needs and financial considerations.Ensure that major equipment and furnishings are maintained in safe, operable condition and/or arrange for replacement. Develop, implement, and review equipment records.Establish procedures and contacts to ensure timely preventive repair of equipment.Secure major equipment bids and make recommendations for purchase when replacement or new equipment is required. Evaluate hazardous conditions and practices and develops hazard control practices and programs, including PPE policies, safe work permitting, and lock out tag out.Establish target areas and long-range accident prevention and cost-control objectives.Additional ResponsibilitiesMay arrange for or provide training for personnel as it relates to the safety or maintenance needs of the organization. This may entail providing staff training in a variety of safety and maintenance topics including the effective utilization of maintenance logs, completion of routine maintenance specific to the facility, safe equipment operations, fire safety training, etc.   qualifications: Experience level: ExperiencedMinimum 5 years of experienceEducation: Bachelors  skills: MEPElectrical Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information
    job summary: Our client in the Newburyport MA area is looking to add an experienced Facilities Engineer to their growing team. Candidates interested should have a minimum of 3 years experience and have electrical controls experience. For further detail and immediate consideration please apply below and call us today. Thank you.   location: NEWBURYPORT, Massachusetts job type: Permanent salary: $110,000 - 125,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Essential Duties and Responsibilities Ensure that building and grounds are maintained in accordance with relevant regulations and fiscal considerations.Evaluate short and long-term needs in relation to major facility projects and property improvements including coordination of contractors.Plan, execute and monitor all facility and property improvement projectsCoordinate, arrange, and supervise the completion of corrective and preventive maintenance actions in accordance with operational needs and financial considerations.Ensure that major equipment and furnishings are maintained in safe, operable condition and/or arrange for replacement. Develop, implement, and review equipment records.Establish procedures and contacts to ensure timely preventive repair of equipment.Secure major equipment bids and make recommendations for purchase when replacement or new equipment is required. Evaluate hazardous conditions and practices and develops hazard control practices and programs, including PPE policies, safe work permitting, and lock out tag out.Establish target areas and long-range accident prevention and cost-control objectives.Additional ResponsibilitiesMay arrange for or provide training for personnel as it relates to the safety or maintenance needs of the organization. This may entail providing staff training in a variety of safety and maintenance topics including the effective utilization of maintenance logs, completion of routine maintenance specific to the facility, safe equipment operations, fire safety training, etc.   qualifications: Experience level: ExperiencedMinimum 5 years of experienceEducation: Bachelors  skills: MEPElectrical Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information

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