MedTech_Sr. RA Specialist_Vision

Johnson & Johnson MedTech; Hong Kong; On-site; HKD 700,000 - 1,000,000; Full time

Job summary

Johnson & Johnson MedTech in Hong Kong is seeking a Senior Regulatory Affairs Specialist (Vision) to lead regulatory activities for HK & Macao, ensuring compliant product registrations and lifecycle management. You will collaborate with commercial, quality, supply chain, and regional RA teams to support launches and tendering, review artwork and labeling, and provide regulatory insights.

This role requires deep knowledge of local requirements and a proactive, cross-functional mindset to

Responsibilities

• Lead dossier prep for HK/Macao registrations and post-approval changes.
• Ensure on-time approvals and renewals before license expiry.
• Prepare and respond to regulatory authority questions promptly.
• Maintain regulatory databases, trackers and archives.
• Monitor regulatory changes in HK/Macao and advise on compliance.
• Review artwork, labeling, and IFUs for HK/Macao.
• Support review of promotional materials per local regulations.
• Provide regulatory input for tendering and act as primary regulatory contact.

Skills

Accountability

Business Behavior

Collaboration

Cross-Functional Work

Stakeholder Management

Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. 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.

Job Function

Regulatory Affairs Group

Job Sub Function

Regulatory Affairs

Job Category

Professional

All Job Posting Locations

Hong Kong, Hong Kong

Job Description

About MedTech

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

About Vision

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 on 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

We are searching for the best talent for Sr. RA Specialist_Vision

Purpose

The Senior Regulatory Affairs Specialist (Hong Kong & Macao) is responsible for leading and executing regulatory activities to ensure compliance, timely product registrations, and lifecycle management of J&J Vision products in Hong Kong and Macao. This role provides regulatory expertise to support product registrations, renewals, promotional activities, and tendering, while ensuring alignment with local regulatory requirements, internal SOPs, and J&J quality standards.

You Will Be Responsible For

Regulatory Submissions & Lifecycle Management

• Lead and take ownership of regulatory dossier preparation for product registrations, renewals, and post‑approval changes in Hong Kong and Macao.
• Be accountable for achieving high‑quality, on‑time approvals for new registrations and changes, and ensuring 100% on‑time renewals prior to license expiry in both markets.
• Prepare, submit, and manage timely responses to regulatory authority questions and official correspondences.
• Maintain accurate regulatory databases, trackers, and archives for all Hong Kong and Macao regulatory documentation.

Regulatory Compliance & Intelligence

• Monitor, interpret, and assess changes in regulatory requirements, legislation, and guidance in Hong Kong and Macao relevant to J&J Vision products.
• Provide regulatory impact assessment, clear interpretations, and practical compliance recommendations to internal stakeholders.
• Ensure ongoing compliance of marketed products throughout their lifecycle in both markets.

Artwork, Labeling & Promotional Material Review

• Review and approve artwork, labeling, packaging, and IFUs to ensure consistency with approved registrations and local regulatory requirements for Hong Kong and Macao.
• Coordinate and support review and approval of promotional and educational materials in compliance with local regulations and internal review processes.

Business & Tendering Support

• Support regulatory inputs for Hong Kong and Macao tendering activities, including review of regulatory sections, compliance statements, and supporting documents.
• Act as the primary regulatory contact for product registration‑related inquiries from health authorities, customers, and internal teams in both markets.

Cross‑Functional Collaboration & Expertise

• Work closely with commercial, quality, supply chain, PD, and regional/global RA teams to support product launches and business continuity in Hong Kong and Macao.
• Serve as a regulatory subject matter expert for the HK & Macao markets.
• Contribute to continuous improvement initiatives, including SOP updates, process optimization, and regulatory best‑practice sharing.

Required Skills

• Accountability
• Business Behavior
• Collaboration
• Cross-Functional Work
• Stakeholder Management

Preferred Skills

• Analytical Reasoning
• Business Writing
• Communication
• Confidentiality
• Data Reporting
• Developing Others
• Inclusive Leadership
• Innovation
• Leadership
• Legal Support
• Medicines and Device Development and Regulation
• Policy Implementation
• Process Improvements
• Productivity Planning
• Product Licensing
• Regulatory Affairs Management
• Regulatory Compliance
• Regulatory Development
• Regulatory Environment