MI
Sr. R&D Engineer (Product Development Activities)
Accepting applicationsMillenniumSoft Inc · Franklin Lakes, NJ
Full-Time Senior
Posted
5d ago
Category
Verification
Experience
Senior
Country
United States
Position: Sr. R&D Engineer (Product Development Activities)
Location : Franklin Lakes, NJ
Duration : 12+ Months contract
Total Hours/week: 40.00
pay rate-$40-55/hr
1st Shift
Client: Medical Device Company
Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)
No H1b’s
Looking for R&D engineers to do product development activities. This is not primarily a testing role.
Description
Demonstrated experience writing complex Design Verification plans, protocols, reports
Proficiency with statistical techniques including Minitab to analysis data, generated appropriate plots/graphs required to show performance against acceptance criteria for DV reports
Ability to write and get cross functional support for engineering rationales used to support product development activities
Demonstrated ability to execute Design Verification testing, including building samples, adherence to test protocols/test methods, responsible data collection/preparation practices, and good lab practices.
Demonstrated ability to clearly and effectively communicate (verbal & written) concepts and ideas to technical and non-technical team members in a way that articulates problem statement, investigating approach, possible solutions, final recommendation, and implementation plan
Strong decision-making capability, even with limited or ambiguous information with the ability to absorb information and solve complex problems quickly
Demonstrated industry or academic experience driving product development in a cross functional team setting to solve complex problems and meet milestones
Works with self-direction, takes initiative, exercises sound judgment, discretion, and capable of complex decision making in a dynamic work environment
Minimum 6 years of experience as a product design / development engineer in the medical device, pharmaceutical or other regulated industry (experience with FDA class II or III medical devices preferred). Bachelor’s degree required in Mechanical or Biomedical Engineering (Mechanics focus). Master Degree or above preferred.
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Location : Franklin Lakes, NJ
Duration : 12+ Months contract
Total Hours/week: 40.00
pay rate-$40-55/hr
1st Shift
Client: Medical Device Company
Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)
No H1b’s
Looking for R&D engineers to do product development activities. This is not primarily a testing role.
Description
Demonstrated experience writing complex Design Verification plans, protocols, reports
Proficiency with statistical techniques including Minitab to analysis data, generated appropriate plots/graphs required to show performance against acceptance criteria for DV reports
Ability to write and get cross functional support for engineering rationales used to support product development activities
Demonstrated ability to execute Design Verification testing, including building samples, adherence to test protocols/test methods, responsible data collection/preparation practices, and good lab practices.
Demonstrated ability to clearly and effectively communicate (verbal & written) concepts and ideas to technical and non-technical team members in a way that articulates problem statement, investigating approach, possible solutions, final recommendation, and implementation plan
Strong decision-making capability, even with limited or ambiguous information with the ability to absorb information and solve complex problems quickly
Demonstrated industry or academic experience driving product development in a cross functional team setting to solve complex problems and meet milestones
Works with self-direction, takes initiative, exercises sound judgment, discretion, and capable of complex decision making in a dynamic work environment
Minimum 6 years of experience as a product design / development engineer in the medical device, pharmaceutical or other regulated industry (experience with FDA class II or III medical devices preferred). Bachelor’s degree required in Mechanical or Biomedical Engineering (Mechanics focus). Master Degree or above preferred.
Show more Show less