Vision R&D Project Specialist

Biopharma Careers; Jacksonville (TX); On-site; USD 90,000 - 120,000; Full time

Job summary

Johnson & Johnson is seeking a Technical Project Specialist in Jacksonville, FL to support R&D and Operations by writing and coordinating protocols for clinical and non-clinical test articles. The role involves multi-disciplinary teamwork to advance vision-related therapies.

You will plan fabrication activities, analyze test data, and contribute to regulatory submissions, while maintaining Design History Records and ensuring compliance with testing requirements.

Qualifications

• Bachelor’s Degree and/or equivalent degree required.
• 2+ years related experience preferred.
• Interface with the Pilot Line, QA, Operations, and management to facilitate test article builds, testing, and release.
• Work in conjunction with project managers and team members to understand expected outcomes and define requirements.
• Provide technical input and guidance for the evaluation of test articles manufactured from new or alternate platforms.

Responsibilities

• Plan, write, and execute test article fabrication of clinical and non-clinical protocols for research projects.
• Gather and analyze insert data, plastic data, and/or lens parameter data for the project teams.
• Create lens parameter, property, biocompatibility, and analytical testing submissions.
• Update and obtain approval of Use and Misuse-Risk Assessment Protocol Tracking to reflect release requirements.
• Organize and assemble Design History Records for protocols run in operations.
• Write and/or revise procedures as needed.

Skills

Analytical Reasoning

Communication

Clinical Data Management

Clinical Operations

Clinical Research

Project Management

Regulatory Knowledge

Study Management

Education

Bachelor’s Degree or equivalent

Job description

Johnson & Johnson is seeking a Technical Project Specialist in Jacksonville, FL to support R&D and Operations by writing and coordinating protocols for clinical and non-clinical test articles. The role involves multi-disciplinary teamwork to advance vision-related therapies.

You will plan fabrication activities, analyze test data, and contribute to regulatory submissions, while maintaining Design History Records and ensuring compliance with testing requirements.