Process Engineer — MedTech Vision Systems

Biopharma Careers; Jacksonville (TX); On-site; USD 85,000 - 120,000; Full time

Job summary

Johnson & Johnson Vision Care, Inc. is seeking a Process Engineer for our Jacksonville, FL site. You will deliver moderately complex engineering projects, support qualification, validation, and change control activities, and partner with Operations to improve yield and reliability.

The role requires a Bachelor’s degree in Engineering, 2–4 years in manufacturing or regulated environments, and strong analytical, writing, and communication skills within GMP/ISO contexts.

Qualifications

• Strong analytical and problem-solving skills.
• Demonstrated technical writing and GDP discipline.
• Effective communication and collaboration skills in matrix environments.
• Working knowledge of project management fundamentals.

Responsibilities

• Plans and executes moderately complex engineering and/or change control projects requiring conceptual evaluation, design, and validation.
• Applies standard project management methodologies to plan work, manage scope, and deliver milestones.
• Participates in technical design reviews and translates requirements into manufacturing, product, or equipment specifications.
• Supports capital and expense project justification as applicable.
• Plans and executes qualification of new or modified equipment, controls, systems, and/or processes; supports vendor and site acceptance testing as required.

Skills

Analytical skills

Technical writing

GDP discipline

Effective communication

Project management

Data analysis tools

Education

Bachelor’s degree in Engineering

Tools

MS Office

Data analysis tools

Job description

Johnson & Johnson Vision Care, Inc. is seeking a Process Engineer for our Jacksonville, FL site. You will deliver moderately complex engineering projects, support qualification, validation, and change control activities, and partner with Operations to improve yield and reliability.

The role requires a Bachelor’s degree in Engineering, 2–4 years in manufacturing or regulated environments, and strong analytical, writing, and communication skills within GMP/ISO contexts.