Senior Regulatory Affairs Program Lead (Robotics & Digital Solutions) - MedTech Surgery, Inc.

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
Regulatory Affairs Group

Job Sub Function:
Regulatory Affairs

Job Category:
Professional

All Job Posting Locations:
Cincinnati, Ohio, United States of America, Santa Clara, California, United States of America

Job Description:

We are searching for the best talent for a Senior Regulatory Affairs Program Lead to support our Robotics & Digital Surgery team.  The preferred location for this role is Cincinnati, OH however Santa Clara, CA is also available as a location.  This role will work a Flex/Hybrid schedule with 3 days per week in-office.  There is NO remote option.  Relocation assistance may be available on a case-by-case basis.

Purpose: In joining our growing regulatory team, the Sr.

Regulatory Affairs Program Lead will help Robotics & Digital Solutions reach US and international regulatory (NPD) approval goals.

Under minimal supervision, the selected candidate will be working on the robotics, instruments and accessories portfolio RA needs, working closely with exceptional engineering and clinical teams, as well as supporting product development stages and generating submission ready documentation and authoring regulatory submissions.

Additionally, this individual will support health authority communications and participate in strategy development.

You Will Be Responsible For:


* Instills and drives a vibrant regulatory culture, working among cross functional groups as a teammate and collaborator.


* Applies strategic regulatory thinking along with technical expertise to develop and implement regulatory strategies for new product clearances and approvals.


* Prepares and submits regulatory information required to obtain global market access, including preparation, writing and filing of FDA submissions (e.g., Q-submissions, IDEs, De Novo, 510(k)s) and global health authorities’ submissions technical documents.


* Serves as a Regulatory Affairs subject matter expert on new product development and engineering design control teams.

This includes conducting reviews and providing expert regulatory feedback for specifications, device testing, risk management, and other relevant documentation in accordance with regulatory requirements and with positioning for regulatory submission.


* Proactively identify issues, effectively communicate timelines for project completion, and address complex issues that may impact registration status.


* Conduct regulatory evaluation of ...