Engineer III
Spectraforce
Branchburg, New Jersey
2 hours ago
Job Description
Job Title: Engineer III
Location: Branchburg, NJ
Duration: 2 Year (Potential Extension)
Hybrid Onsite Schedule, in office Tue, Wed, Th, with the ability to be remote Mon, Fri. If business needs require on-site presence Mon/Fri it may be necessary.
Responsibilities:
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
• Serve on project technical team, consisting of cross-functional resources including but not limited to R&D, PDS&T, Quality, Biocompatibility, and Regulatory.
• Partner with R&D to identify user and technical product requirements for a medical device product.
• With Technical Lead, Develop Design Verification & Validation strategy.
o Support Design Verification (planning, fixture development, method development, test method validation, protocol development, and test execution).
• Drive the creation and execution of protocols and reports.
• Manage Design History File content.
• Participate in prototyping activities to transform concepts into functional devices.
• Perform laboratory testing, including independently designed experiments to further project goals.
• Conduct statistical analyses using software such as MiniTab or JMP to evaluate data and support design decisions.
• Ensure compliance with company and industry standards regarding safety, quality, and regulatory policies (including GxP).
Qualifications:
List required and preferred qualifications (up to 10). Include education, skills and experience.
• Experience with new product development, including defining user and technical product requirements.
• Experience with Design controls, including Design Verification & Validation strategy development and execution.
• Experience with laboratory testing as well as subsequent data analysis using statistical methods.
• Experience with medical device regulatory submissions.
• Experience with biological-based products preferred.
• Bachelor’s Degree or equivalent education with 5 or more years of experience or Master’s degree or equivalent education with 3 or more years of experience.
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 65.00/hr.
Location: Branchburg, NJ
Duration: 2 Year (Potential Extension)
Hybrid Onsite Schedule, in office Tue, Wed, Th, with the ability to be remote Mon, Fri. If business needs require on-site presence Mon/Fri it may be necessary.
Responsibilities:
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
• Serve on project technical team, consisting of cross-functional resources including but not limited to R&D, PDS&T, Quality, Biocompatibility, and Regulatory.
• Partner with R&D to identify user and technical product requirements for a medical device product.
• With Technical Lead, Develop Design Verification & Validation strategy.
o Support Design Verification (planning, fixture development, method development, test method validation, protocol development, and test execution).
• Drive the creation and execution of protocols and reports.
• Manage Design History File content.
• Participate in prototyping activities to transform concepts into functional devices.
• Perform laboratory testing, including independently designed experiments to further project goals.
• Conduct statistical analyses using software such as MiniTab or JMP to evaluate data and support design decisions.
• Ensure compliance with company and industry standards regarding safety, quality, and regulatory policies (including GxP).
Qualifications:
List required and preferred qualifications (up to 10). Include education, skills and experience.
• Experience with new product development, including defining user and technical product requirements.
• Experience with Design controls, including Design Verification & Validation strategy development and execution.
• Experience with laboratory testing as well as subsequent data analysis using statistical methods.
• Experience with medical device regulatory submissions.
• Experience with biological-based products preferred.
• Bachelor’s Degree or equivalent education with 5 or more years of experience or Master’s degree or equivalent education with 3 or more years of experience.
Applicant Notices & Disclaimers
- For information on benefits, equal opportunity employment, and location-specific applicant notices, click here
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 65.00/hr.