Technical Project Specialist

Johnson & Johnson Innovative Medicine • Jacksonville, FL

3d • Onsite

About The Position

We are searching for the best talent to join our Vision team as a Technical Project Specialist located in Jacksonville, FL. Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

Requirements

• Bachelor’s Degree and/or equivalent degree required

Nice To Haves

• 2+ years related experience preferred
• Ability to travel up to 10%

Responsibilities

• Writes, oversees and facilitates protocols to produce clinical and non-clinical test articles in support of R&D and Operations initiatives.
• Works as an active participant in multi-disciplinary teams involved in test article research and development.
• Provides technical assistance to project teams.
• Provides clarification and/or resolution to project challenges.
• Communicates and facilitates required testing for release of test articles to the clinic.
• Writes and coordinates technical protocols and/or reports in support of stability studies and regulatory submissions.
• Organizes and assembles Design History Records for protocols run in operations.
• Gathers and analyzes test article data in support of research projects.
• 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.
• 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.

Benefits

• We provide an inclusive work environment where each person is considered as an individual.
• At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level