Job Title: Nuclear Medicine Test Professional (SIMNJP) Duration: 12 months contract to start Location: Hoffman Estates IL USA 60195 Candidate must be able to work onsite. Pay rate: $50/hr on W2 Schedule: 40 hr work week. 8:30am - 5:00pm Job Description: This is a role well suited to an ambitious Nuclear Medicine professional, looking for the next step in their career. We are seeking a strategic and critical thinker with a strong technical background. As a Nuclear Medicine Test Professional, you will be responsible for: • Applying your Nuclear Medicine background to execute manual informal and formal Verification and Validation testing of complex nuclear medicine scanners and applications, while providing thorough and timely feedback to the development team on observations. • Identifying, submitting, tracking, and validating product defects using industry-standard tools. • Reporting on the quality, maturity, and progress of Nuclear Medicine products/documentation content to test leads. • Monitoring the status of planned tasks within assigned scope of work and ensuring commitments are on track, while resolving dynamic challenges and conflicts. • Analyzing system requirements and technical concept specifications to ensure adequate functionality coverage. • Analyzing customer feedback and supporting customer complaint investigations. • Interacting with internal stakeholders such as support representatives, developers, technical writers, product managers, project managers, and quality assurance colleagues. • Maintaining prototypes in the lab in a manner as they would be used in a clinical environment, including troubleshooting issues and providing resolutions. • Supporting software installation, configuration, and quality control calibration of systems. • Taking part in the knowledge exchange within our R&D team to improve and further develop our products and software solutions. This position may suit you best if you possess the below-mentioned attributes. • Proficient with performing SPECT and SPECT/CT acquisitions in a clinical environment. • Broad clinical application experience processing nuclear medicine scans. • Hands on Quality Control experience on SPECT and SPECT/CT systems. • Conversant in handling radioactive material on a regular basis. • Ability to solve problems quickly and completely. • Ability to multi-task and stay organized in a dynamic environment. • Demonstrated ability to work in a fast-paced, team-focused environment with minimal supervision. Required skills to have for the success of this role: • Bachelor's Degree in Nuclear Medicine Technology or related disciplines. • Strong understanding of nuclear medicine and computer tomography clinical protocols.
06/03/2026
Full time
Job Title: Nuclear Medicine Test Professional (SIMNJP) Duration: 12 months contract to start Location: Hoffman Estates IL USA 60195 Candidate must be able to work onsite. Pay rate: $50/hr on W2 Schedule: 40 hr work week. 8:30am - 5:00pm Job Description: This is a role well suited to an ambitious Nuclear Medicine professional, looking for the next step in their career. We are seeking a strategic and critical thinker with a strong technical background. As a Nuclear Medicine Test Professional, you will be responsible for: • Applying your Nuclear Medicine background to execute manual informal and formal Verification and Validation testing of complex nuclear medicine scanners and applications, while providing thorough and timely feedback to the development team on observations. • Identifying, submitting, tracking, and validating product defects using industry-standard tools. • Reporting on the quality, maturity, and progress of Nuclear Medicine products/documentation content to test leads. • Monitoring the status of planned tasks within assigned scope of work and ensuring commitments are on track, while resolving dynamic challenges and conflicts. • Analyzing system requirements and technical concept specifications to ensure adequate functionality coverage. • Analyzing customer feedback and supporting customer complaint investigations. • Interacting with internal stakeholders such as support representatives, developers, technical writers, product managers, project managers, and quality assurance colleagues. • Maintaining prototypes in the lab in a manner as they would be used in a clinical environment, including troubleshooting issues and providing resolutions. • Supporting software installation, configuration, and quality control calibration of systems. • Taking part in the knowledge exchange within our R&D team to improve and further develop our products and software solutions. This position may suit you best if you possess the below-mentioned attributes. • Proficient with performing SPECT and SPECT/CT acquisitions in a clinical environment. • Broad clinical application experience processing nuclear medicine scans. • Hands on Quality Control experience on SPECT and SPECT/CT systems. • Conversant in handling radioactive material on a regular basis. • Ability to solve problems quickly and completely. • Ability to multi-task and stay organized in a dynamic environment. • Demonstrated ability to work in a fast-paced, team-focused environment with minimal supervision. Required skills to have for the success of this role: • Bachelor's Degree in Nuclear Medicine Technology or related disciplines. • Strong understanding of nuclear medicine and computer tomography clinical protocols.
APN Software Services, Inc.
Cambridge, Massachusetts
Job Title - CAPA Quality Engineer Location - Cambridge MA Length - Contract (11 Months+) Job Responsibilities: Facilitate product and process Corrective and Preventive Action (CAPA) investigations from issue identification through implementation of solution and effectiveness monitoring. Project manage all aspects of CAPA activity which includes gaining the commitment of cross functional resources, scheduling CAPA team meetings, and ensuring CAPA deliverables per project timelines. Represent CAPAs during audits and CAPA Review Board meetings. Lead and mentor cross functional teams with the implementation of appropriate root cause analysis techniques (e.g. Pride problem solving). Analyze quality monitoring data sources and apply statistical techniques to identify existing and potential causes of non-conformances. Work effectively with all levels of management to ensure CAPA action plans can be supported and that costs/resources needed to implement the plan are available. • Independently produces and completes CAPA (Corrective and Preventive Action) records. • Responsible for performing timely, detailed CAPA engineering tasks like assessing issue descriptions, reviewing CAPA data sources, assisting with root cause analysis, and quality problem-solving. Able to understand and analyze complex problems, including software and hardware design issues. Demonstrated knowledge of tools and techniques required to perform thorough root cause analysis and develop strong investigations. Strong understanding of appropriate global regulations, requirements, and standards such as 21 CFR Parts 803, 806, and 820, ISO 13485, ISO 9001 and ISO 14971. Demonstrated ability to partner with the business and effectively interact with and influence employees, and managers on all levels. Strong Project Management skills, including ability to project manage all CAPA activities. Ability to analyze data and apply statistical techniques. Koninklijke Philips N.V. Job Family Description Excellent written and verbal communication skills Responsible for leading CAPA engineering activities like: assessing complex investigations and corrective actions and reviewing test and other complex performance data, leading complex root cause analysis and complex quality problem solving. Bachelor's engineering degree with > 5 years of related experience, or a Master's degree with > 3 years of related experience. Position Details: • These critical resources are being added to support the injunction lift and getting the CAPA program back to a healthy state.
06/03/2026
Full time
Job Title - CAPA Quality Engineer Location - Cambridge MA Length - Contract (11 Months+) Job Responsibilities: Facilitate product and process Corrective and Preventive Action (CAPA) investigations from issue identification through implementation of solution and effectiveness monitoring. Project manage all aspects of CAPA activity which includes gaining the commitment of cross functional resources, scheduling CAPA team meetings, and ensuring CAPA deliverables per project timelines. Represent CAPAs during audits and CAPA Review Board meetings. Lead and mentor cross functional teams with the implementation of appropriate root cause analysis techniques (e.g. Pride problem solving). Analyze quality monitoring data sources and apply statistical techniques to identify existing and potential causes of non-conformances. Work effectively with all levels of management to ensure CAPA action plans can be supported and that costs/resources needed to implement the plan are available. • Independently produces and completes CAPA (Corrective and Preventive Action) records. • Responsible for performing timely, detailed CAPA engineering tasks like assessing issue descriptions, reviewing CAPA data sources, assisting with root cause analysis, and quality problem-solving. Able to understand and analyze complex problems, including software and hardware design issues. Demonstrated knowledge of tools and techniques required to perform thorough root cause analysis and develop strong investigations. Strong understanding of appropriate global regulations, requirements, and standards such as 21 CFR Parts 803, 806, and 820, ISO 13485, ISO 9001 and ISO 14971. Demonstrated ability to partner with the business and effectively interact with and influence employees, and managers on all levels. Strong Project Management skills, including ability to project manage all CAPA activities. Ability to analyze data and apply statistical techniques. Koninklijke Philips N.V. Job Family Description Excellent written and verbal communication skills Responsible for leading CAPA engineering activities like: assessing complex investigations and corrective actions and reviewing test and other complex performance data, leading complex root cause analysis and complex quality problem solving. Bachelor's engineering degree with > 5 years of related experience, or a Master's degree with > 3 years of related experience. Position Details: • These critical resources are being added to support the injunction lift and getting the CAPA program back to a healthy state.
