Johnson & Johnson Posted October 13, 2026

Assistant RA Manager

Beijing, China Full time
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About this opportunity

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 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:

Beijing, China

Job Description:

Key Responsibilities:

Class II & III new, change, renewal and filing registration Accountabilities:

1. Directs both growth/innovation and post-marketing Lifecycle Management (LCM) Regulatory activities (e.g., claims, change management, renewals, copy clearance, global LCM labeling support, and external environment surveillance).

2. Oversees the creation of global regulatory product development strategies and preparation/submission of marketing approval applications to health authorities to ensure that development plans meet global regulatory requirements.

3. Ensure compliance with product post-marketing approval requirements.

4. Interacts with internal regulatory personnel, external trade association partners, and regulators to resolve regulatory matters ranging from pending application negotiations to proposed legislation and guidance document ramifications for the business. Participate in applicable trade association/industry working groups to influence policy in alignment with business strategies.

5. Anticipate emerging issues and develop solutions.

Other Duties

1 Analyze and compare regulatory outcomes with initial product concepts and recommend future strategies and actions

2 Integrate regulatory considerations into the corporation’s global product entry and exit strategy

3 Recruit, develop, and mentor regulatory professionals

4 Communicate application progress to internal stakeholders

5 Provide regulatory input for follow-up to inspections and audits to minimize potential for findings of noncompliance

6 Represent regulatory affairs in product recall and recall communication process

7 Manage processes involved with maintaining annual licenses, registrations, listings, and patent information

8 Labelling Accountabilities: Review, copy clear and maintain JJVC product labelling including local carton and Instructions for use in compliance with country specific regulation.

Qualifications

Education:

At least Bachelor’s Degree or equivalent experience, preferably majored in scientific, technical, or engineering; MD is preferred

Experience and Skills:

Required:

Minimum 6 years experience in medical device industry with hands on NPI experience obtaining regulatory approvals for medical devices

Skilled in establishing collaboration with internal and external partners, successfully influence functional business partners

A strong self-learner and Critical thinking with hands on knowledge and skill

Proficient communication and social skills

Sense of collaboration

Preferred:

Experience in the field of class III active medical devices

Other:

Language Requirements: Proficient speaking in English

Travel Requirements: 10%

Required Skills:

Preferred Skills:

Business Writing, Compliance Risk, Developing Others, Fact-Based Decision Making, Inclusive Leadership, Industry Analysis, Innovation, Leadership, Legal Support, Operations Management, Policy Development, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Development, Regulatory Environment, Strategic Thinking, Team Management

Job details

Seniority
Manager
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Beijing, China
Employment type
Full time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 248 comparable Manager Regulatory Affairs roles across 68 biopharma companies.

248Comparable roles tracked
224Currently active
68Companies hiring similar roles
30Countries represented

Salary context

79 of 248 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Manager, Strategy and Operations · Johnson & Johnson $102,000/yr – $177,100/yr
Peer group range $139,550 – $208,845 (median $180,500)

Where these roles are based

Top locations among the 248 comparable roles

United States106
India28
Japan18
United Kingdom15
Poland14
Ireland11

+ 24 more countries

Seniority mix

248 of 248 peers have a known seniority level

Manager180
Associate Director55
Associate13

Therapeutic area mix

25 of 248 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology9
Immunology8
Dermatology & Aesthetics5
Vaccines & Infectious Disease1
Respiratory1
Rare Disease1

Currently open similar roles

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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Johnson & Johnson · Shanghai, China · Manager
Function Therapeutic area Seniority Country
60%
Senior Manager, Regulatory Affairs
AbbVie · Beijing, Beijing · Manager
Function Therapeutic area Seniority Country
50%
Assoc Director, Regulatory Affairs China - Immunology
Johnson & Johnson · Beijing, China · Associate Director
Function Therapeutic area Adjacent seniority Country
45%
Senior Manager, Core Labeling Strategy
Mylan Inc. · Washington, United States · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.