Regulatory Affairs Analyst

Regulatory Affairs Analyst

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.

Your unique talents will help patients on their journey to wellness. Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.

Duties / Responsibilities :

• Project management by maintaining multiple tracking logs for tracking and reporting project status and resource availability
• Maintaining compliance pertaining to Medical Device Listings and Establishment Registrations
• Effectively initiate, track, and monitor purchase orders and invoices to ensure payments are processed in the company electronic systems in a timely manner
• Coordinate logistics for internal and external audits, including on-site and desk audits
• Assist with general department responsibilities, such as setting up department meetings, archiving physical and electronic documentation, coordinating regulatory submissions locally and internationally, tracking submission details and metrics, distributing department communication, etc.
• Monitor and respond to international requests
• Arrange logistics for international visits
• Perform other job-related duties as assigned

Qualifications / Requirements :

Additional Information :

This job posting is anticipated to close on October 25, 2025. The Company may however extend this time-period, in which case the posting will remain available on to accept additional applications.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via or contact AskGS to be directed to your accommodation resource.