Job Function:
R&D Operations
Job Sub Function:
Clinical/Medical Operations
Job Category:
Professional
All Job Posting Locations:
Jacksonville, Florida, United States of America
Job Description:
We are searching for the best talent to join our Vision team as a Technical Project Specialistlocated in Jacksonville, FL.
Fueled by innovation at the intersection of biology and technology, we27re 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 that27s 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 6 from the pediatric to aging eye 6 in a patient27s lifetime.
Your unique talents will help patients on their journey to wellness. Learn more at
Purpose: The Technical Project Specialist 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.
You will:
- 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.
Qualifications
- Bachelor27s 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
Other:
- Ability to travel up to 10%
**A pre-identified candidate for consideration has been identified. However, all applications will be considered**
#LI-AM2
Required Skills:
Preferred Skills:
Analytical Reasoning, Business Behavior, Clinical Data Management, Clinical Operations, Clinical Research and Regulations, Clinical Trial Designs, Clinical Trials Operations, Communication, Ethical and Participant Safety Considerations, Execution Focus, Innovation, Laboratory Operations, Office Administration, Preclinical Research, Project Management, Research and Development, Study Management
