Manufacturing Engineer – MedTech Vision Systems

Biopharma Asia; Jacksonville (FL); On-site; USD 70,000 - 100,000; Full time

Job summary

Johnson & Johnson Vision Care, Inc. in Jacksonville, FL is recruiting for an Engineer to join the Vision team in Manufacturing Engineering.

The role focuses on supporting medical device eye-care product development and production improvements in a regulated environment. You will operate within ISO and FDA-regulated processes, collaborating with safety, quality, and operations to ensure compliance and device performance.

Qualifications

• Bachelor’s degree in Engineering or equivalent.
• 2–4 years of engineering experience.
• Strong written and verbal communication skills.
• Ability to work in an empowered work team environment.
• Experience in ISO and FDA regulated environment preferred.

Responsibilities

• Plans and executes moderately complex change control projects requiring conceptual evaluation, design and validation.
• Plans and executes moderately complex qualification of new equipment/controls and assists in vendor and site acceptance testing to meet engineering standards.
• Identifies and implements standard methodologies of project management.
• Participates in technical design reviews for machine requirements and manufacturing/product specifications.
• Provides training and support to Operations Engineers and Technicians to operate, troubleshoot and maintain equipment.
• Identification and resolution of Corrective/Preventative actions (NCRs, CAPAs, etc.).
• Utilizes cross functional collaboration with safety, quality, and operations to meet business objectives.

Skills

Communication

Teamwork

GMP

Lean manufacturing

Education

Bachelor’s degree in Engineering

Job description

Johnson & Johnson Vision Care, Inc. in Jacksonville, FL is recruiting for an Engineer to join the Vision team in Manufacturing Engineering.

The role focuses on supporting medical device eye-care product development and production improvements in a regulated environment. You will operate within ISO and FDA-regulated processes, collaborating with safety, quality, and operations to ensure compliance and device performance.