Job Description

Johnson & Johnson Surgical Vision (JJSV) is recruiting for a Project Manager, Regulatory Affairs (Specialist IV) in Santa Ana, CA or remote for the right candidate (in the US).

JJSV designs, manufactures, and distributes products designed for the evaluation, imaging, and treatment of Meibomian Gland Dysfunction (MGD), the leading cause of dry eye and ocular surface disease (OSD), and for the surgical treatment of anterior segment ophthalmic disorders, most notably cataract removal.

Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 125 years. We embrace research and science -- bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.

The Johnson & Johnson Surgical Vision goal is improving sight throughout a patients lifetime. J&J; Surgical Vision is well positioned to address a full range of vision health needs for global markets: The No. 2 global provider of CATARACT products and a leader in presbyopia-correcting IOLs, the Global REFRACTIVE (LASIK) market leader, and leading innovator in addressing MGD, a major contributor to dry eye, all supported with a CONSUMER EYE HEALTH diverse portfolio of solutions and drops. Johnson & Johnson Surgical Vision has operations in the United States, Latin America, Asia-Pacific and Europe/Middle East/Africa regions. Research, innovation and new-product development are the focus of our organization. Our associates around the world are committed to expanding our brands and fortifying our position as the worldwide leader in the industry.

The Project Manager, Regulatory Affairs will provide independent regulatory guidance to new product development and Value Stream teams in strategic planning, pre-marketing, and related submissions to support optimal timelines for new/modified product launches including defining data and information needed for regulatory approvals in conjunction with cross-functional business partners. As part of project management, you may be called upon to manage other team members.

In this role, you will:

* Be responsible for providing regulatory guidance to project teams and will be responsible for assessing device/manufacturing changes, developing regulatory strategies and writing/coordinating/compiling and submitting regulatory documents to FDA and other Regulatory Agencies.
* Create and maintain documents including PMA/PMA Supplements/30 Day Notices, IDEs, 510(k) submissions, Change Notifications, Technical Files/Design Dossiers (CE Mark) and responses to regulatory agencies questions and other correspondence.
* Act as regulatory liaison to U.S. Food & Drug Administration for regulatory submissions and other projects as required
* Work with cross-functional teams to enable the integration of existing Tear Sciences (TS) products and enable incremental changes and new or emerging technologies
* Effectively lead and collaborate with colleagues, OUS Affiliates, and external partners where required to ensure team objectives and milestones are met in a timely manner.
* Ensure compliance with regulatory agency regulations and interpretations.
* Develop timelines for submissions under the direction of senior regulatory affairs staff.
* Develop solutions to a variety of problems of high scope and complexity.
* Participate in the development, review and approval of product labeling.
* Perform other duties as assigned by the manager of this position.

Qualifications
* A Bachelors Degree and a minimum of 6 years related work experience in a regulated industry and an Advanced Degree and a minimum of 4 years related work experience in a regulated industry is required.
* Knowledge of Title 21 of the US Code of Federal Regulations (21 CFR 800-1299) is required.
* Experience with US Federal Food, Drug, and Cosmetic Act (FD&C;) is required.
* Experience with 510(k) required.
* Experience PMA-related submissions preferred.
* Experience with European Medical Devices Directive (93/42/EEC) is required.
* Knowledge EU MDR (2007/47/EC) is preferred.
* Experience with of Quality Management System Standard ISO 13485 is required.
* Knowledge of International Medical Device requirements and submission experience (China, Japan, Canada, Australia, Brazil, Russia, etc.) is preferred.
* Knowledge of software regulations is preferred.
* Excellent written and oral communication skills are required.
* Good analytical thinking, problem solving, and investigative skills are required.
* Proficiency in Microsoft Office and all related applications is required.
* This position will be located in Santa Ana, CA or remote for the right candidate (in the US) and may require up to 20% domestic and/or international travel.

Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

Primary Location
United States-California-Santa Ana-1700 E Saint Andrew Place
Other Locations
United States
Organization
AMO Development, LLC (6242)
Job Function
Regulatory Affairs
Requisition ID
2105888650W