R&D Engineer

CS&S STAFFING SOLUTIONS; New York (NY); On-site; USD 100,000 - 130,000; Full time

Job summary

A leading manufacturer of Medical Devices in New York is seeking a Staff R&D Engineer. The R&D Engineer will lead the New Product Development process and mentor junior engineers, ensuring compliance with FDA regulations. Candidates should have a BS in Mechanical or Biomedical Engineering and 6-12 years of experience in this field. Excellent communication skills and a track record of solving complex design problems are essential. This position offers the opportunity to contribute significantly to product innovation.

Qualifications

• 6-12 years of new product development experience in an FDA regulated medical device environment.
• Demonstrated ability to solve complex design and engineering problems.
• Experience building experimental test set-ups to assess functional performance.

Responsibilities

• Identify and analyze design problems to achieve optimal solutions.
• Lead development of product specifications and conduct design reviews.
• Ensure project deliverables meet global requirements.

Skills

Six Sigma

Problem-solving

Excellent communication skills

Education

BS in Mechanical or Biomedical Engineering

Masters or PhD preferred

Tools

Metal and plastic injection molding

Job description

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Job Description

Our client is a leading manufacturer of Medical Devices, seeking a Staff R&D Engineer to join their team on Long Island, NY. The R&D Engineer will lead cradle to launch New Product Development and existing product improvement initiatives. The R&D Engineer will be responsible for the development of specifications and leading design activities. This is a technical engineering role that requires investigation of new processes and application of advanced engineering methodologies. The R&D Engineer will work in a cross-functional team environment and will oversee and mentor junior engineers.

Responsibilities

• Identifies and analyzes design problems to achieve optimal solutions that satisfy technical requirements, using internal and external technical resources
• Formulates new, innovative approaches to solve technical problems on a consistent basis
• Uses Six Sigma or other process improvement methodologies
• Leads development of product specifications, risk documents and conducts technical and design reviews
• Ensures that project deliverables meet global requirements (regulatory, etc.)
• Supports and participated during internal and external audits

Requirements

• BS in Mechanical or Biomedical Engineering, Masters or PhD preferred
• 6-12 years of new product development experience in an FDA regulated medical device or pharmaceutical environment using stage-gate development process (candidates with an advanced degree may have fewer years of experience)
• Knowledge of metal and plastic injection molding a plus
• Demonstrated ability to solve complex design and engineering problems
• Experience building experimental test set-ups to characterize and assess functional performance of medical products
• Six Sigma Black Belt a plus
• Excellent communication skills needed

Additional Information

All your information will be kept confidential according to EEO guidelines.