Engineer II, R&D Sustaining & Value Engineering

Becton Dickinson; Nampa (ID); On-site; USD 70,000 - 100,000; Full time

Job summary

Becton Dickinson seeks an Engineer II to support lifecycle management and continuous improvement of commercialized medical devices. You will engage in sustaining activities, value engineering projects, and cross-functional collaboration to optimize cost, manufacturability, and reliability.

The role requires a Bachelor’s degree in engineering or related field and 3–5 years of medical device experience, with strong analytical and communication skills and knowledge of regulatory standards.

Qualifications

• Bachelor's degree in Engineering or related field.
• 3–5 years of engineering experience, preferably in medical devices.
• Strong analytical and problem-solving capabilities.
• Experience with value analysis/value engineering (VAVE) projects.
• Knowledge of regulatory standards and quality system requirements.

Responsibilities

• Support sustaining engineering activities for medical device products.
• Execute value analysis and value engineering projects focused on cost reduction.
• Develop and implement design changes to improve manufacturability and reliability.
• Perform engineering analyses, root cause investigations, and risk assessments.
• Author design control documentation and maintain technical records.

Skills

Analytical thinking

Problem-solving

Communication skills

Regulatory knowledge

Education

Bachelor's degree in Engineering or related field

Job description

Becton Dickinson seeks an Engineer II to support lifecycle management and continuous improvement of commercialized medical devices. The role involves sustaining engineering, value engineering projects, and cost optimization while ensuring regulatory compliance and cross-functional collaboration.

Responsibilities

• Support sustaining engineering activities for commercialized medical device products
• Execute value analysis and value engineering projects focused on cost reduction
• Develop and implement design changes to improve manufacturability and reliability
• Perform engineering analyses, root cause investigations, and risk assessments
• Author design control documentation and maintain technical records

Requirements

• Bachelor's degree in Engineering or related field
• 3-5 years of engineering experience, preferably in medical devices
• Strong analytical and problem-solving capabilities
• Experience with value analysis/value engineering (VAVE) projects
• Demonstrated ability to implement design changes and improvements
• Excellent written and verbal communication skills
• Knowledge of regulatory standards and quality system requirements