A-Line Staffing Solutions
Research And Development Engineer
A-Line Staffing Solutions, Franklin Lakes, New Jersey, us, 07417
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A-Line Staffing Solutions provided pay range This range is provided by A-Line Staffing Solutions. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $55.00/hr - $60.00/hr
Direct message the job poster from A-Line Staffing Solutions
R&D Senior Engineer – Specimen Management / Medical Devices Position Overview We are seeking an experienced
R&D Senior Engineer
to serve as a key contributor within a Research & Development team supporting a
Specimen Management / Specimen Acquisition Platform . This role requires advanced engineering expertise, strong technical judgment, and the ability to independently solve complex product development challenges in a regulated medical device environment.
The ideal candidate works under general direction, determines technical approaches independently, contributes to projects of significant impact, and may lead smaller-scope initiatives. This position plays a critical role in design, testing, verification, validation, and risk-based product development.
Key Responsibilities Product Development & Technical Leadership
Contribute to R&D projects of considerable scope or lead smaller engineering initiatives.
Independently determine and develop technical approaches to solve complex engineering problems.
Apply sound engineering principles to deliver imaginative, practical, and data-driven solutions.
Support material, design, and process changes through formal
design control processes , ensuring timely and successful completion of assigned work.
Design, Testing & Validation
Design and develop
in vivo and in vitro models
to evaluate product features and improvements.
Plan, execute, and analyze
Design of Experiments (DOE) .
Develop robust test methods, design test fixtures, and perform
Measurement System Analysis (MSA) .
Execute and document
bench studies, tolerance stack-up analyses, design verification, and validation
activities.
Support vendor interactions, materials selection, and component specifications.
Data Analysis & Reporting
Perform statistical analysis, regression analysis, and develop transfer functions.
Collect, record, interpret, and analyze experimental data.
Prepare technical reports and present findings to peers and business leadership.
Provide advanced engineering input to support business cases for new product opportunities.
Quality & Compliance
Ensure compliance with quality system requirements, policies, and procedures.
Apply risk-based development approaches aligned with medical device regulations.
Promote quality awareness and sound engineering practices across the team.
Cross-Functional Collaboration
Participate in and lead technical, DFSS, design, and cross-functional reviews.
Direct associates and lead small cross-functional groups when required.
Collaborate with manufacturing, quality, supply chain, and external partners.
Required Knowledge & Skills Engineering & Technical Expertise
Strong knowledge of
engineering first principles .
Proven technical judgment and problem-solving abilities.
Experience with
R&D functional planning, requirement generation, and technical reviews
across all product development phases.
Proficiency with
solid modeling tools
such as
Pro/ENGINEER (Creo), SolidWorks , or equivalent.
Proficiency in
fixture design , basic machining considerations, and test method development.
Understanding of
high-volume, tightly controlled manufacturing processes .
Methodologies & Quality Systems
Strong understanding of
Six Sigma (DMAIC)
and
Design for Six Sigma (DFSS)
methodologies.
Knowledge of
Measurement Systems Analysis (MSA) .
Experience working within
phase-gate product development processes .
Strong project management, prioritization, and multitasking skills.
Ability to work independently with minimal direction.
Experience leading small cross-functional teams or directing associates.
Proficiency with
Microsoft Project
or similar project planning tools.
Communication
Excellent written and verbal communication skills.
Ability to clearly communicate technical concepts, risks, and recommendations to diverse audiences.
Preferred Qualifications
Experience in the
medical device or life sciences industry .
Hands‑on experience with statistical tools and experimental analysis software.
Experience supporting supplier development and component qualification.
Seniority level
Mid‑Senior level
Employment type
Contract
Job function
Medical Equipment Manufacturing
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A-Line Staffing Solutions provided pay range This range is provided by A-Line Staffing Solutions. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $55.00/hr - $60.00/hr
Direct message the job poster from A-Line Staffing Solutions
R&D Senior Engineer – Specimen Management / Medical Devices Position Overview We are seeking an experienced
R&D Senior Engineer
to serve as a key contributor within a Research & Development team supporting a
Specimen Management / Specimen Acquisition Platform . This role requires advanced engineering expertise, strong technical judgment, and the ability to independently solve complex product development challenges in a regulated medical device environment.
The ideal candidate works under general direction, determines technical approaches independently, contributes to projects of significant impact, and may lead smaller-scope initiatives. This position plays a critical role in design, testing, verification, validation, and risk-based product development.
Key Responsibilities Product Development & Technical Leadership
Contribute to R&D projects of considerable scope or lead smaller engineering initiatives.
Independently determine and develop technical approaches to solve complex engineering problems.
Apply sound engineering principles to deliver imaginative, practical, and data-driven solutions.
Support material, design, and process changes through formal
design control processes , ensuring timely and successful completion of assigned work.
Design, Testing & Validation
Design and develop
in vivo and in vitro models
to evaluate product features and improvements.
Plan, execute, and analyze
Design of Experiments (DOE) .
Develop robust test methods, design test fixtures, and perform
Measurement System Analysis (MSA) .
Execute and document
bench studies, tolerance stack-up analyses, design verification, and validation
activities.
Support vendor interactions, materials selection, and component specifications.
Data Analysis & Reporting
Perform statistical analysis, regression analysis, and develop transfer functions.
Collect, record, interpret, and analyze experimental data.
Prepare technical reports and present findings to peers and business leadership.
Provide advanced engineering input to support business cases for new product opportunities.
Quality & Compliance
Ensure compliance with quality system requirements, policies, and procedures.
Apply risk-based development approaches aligned with medical device regulations.
Promote quality awareness and sound engineering practices across the team.
Cross-Functional Collaboration
Participate in and lead technical, DFSS, design, and cross-functional reviews.
Direct associates and lead small cross-functional groups when required.
Collaborate with manufacturing, quality, supply chain, and external partners.
Required Knowledge & Skills Engineering & Technical Expertise
Strong knowledge of
engineering first principles .
Proven technical judgment and problem-solving abilities.
Experience with
R&D functional planning, requirement generation, and technical reviews
across all product development phases.
Proficiency with
solid modeling tools
such as
Pro/ENGINEER (Creo), SolidWorks , or equivalent.
Proficiency in
fixture design , basic machining considerations, and test method development.
Understanding of
high-volume, tightly controlled manufacturing processes .
Methodologies & Quality Systems
Strong understanding of
Six Sigma (DMAIC)
and
Design for Six Sigma (DFSS)
methodologies.
Knowledge of
Measurement Systems Analysis (MSA) .
Experience working within
phase-gate product development processes .
Strong project management, prioritization, and multitasking skills.
Ability to work independently with minimal direction.
Experience leading small cross-functional teams or directing associates.
Proficiency with
Microsoft Project
or similar project planning tools.
Communication
Excellent written and verbal communication skills.
Ability to clearly communicate technical concepts, risks, and recommendations to diverse audiences.
Preferred Qualifications
Experience in the
medical device or life sciences industry .
Hands‑on experience with statistical tools and experimental analysis software.
Experience supporting supplier development and component qualification.
Seniority level
Mid‑Senior level
Employment type
Contract
Job function
Medical Equipment Manufacturing
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