Assistant RA Manager
We couldn't confirm this posting on Johnson & Johnson's site in our latest checks -- see current similar openings below.
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
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.
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.
Where these roles are based
Top locations among the 248 comparable roles
+ 24 more countries
Seniority mix
248 of 248 peers have a known seniority level
Therapeutic area mix
25 of 248 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
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.
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.