Sr Director, Head of Biologics China Core
3/10/2026
This role is responsible for leading the China Biologics Core function, which includes API, DPD, and AD teams, to support product launches and ongoing commercial operations in China. Essential duties involve shaping Chinese regulatory strategy through direct engagement with health authorities and ensuring rigorous oversight of technical development and GMP operations at China-based CDMOs/CROs.
Working Hours
40 hours/week
Company Size
10,001+ employees
Language
English
Visa Sponsorship
No
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:
R&D Product DevelopmentJob Sub Function:
R&D Chemical/Biochemical EngineeringJob Category:
People LeaderAll Job Posting Locations:
Shanghai, ChinaJob Description:
An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.
Position Summary
Provide brief and concise statement explaining the main purpose for the existence of this position. Provide a brief summary of the role.
• Lead the China Biologics Core function including China based API, DPD, and AD teams.
• Collaborates internally with Commercial Operation, Regulatory, Quality, IMSC, and other partnering Protein Development functions and externally with Chinese health authorities to drive products launch and ongoing commercial operation in China.
• Shape Chinese regulatory strategy through direct projects with Chinese health authorities, engagement on Chinese healthcare regulations, industry forums, participation at meetings, and publications & presentations. This is a critical activity as Chinese regulatory policies are changing rapidly.
• Ensure rigorous oversight of technical development and GMP operation at CDMOs and CROs based in China. Ensure on time and on quality support of Technical Transfer between China based CDMOs / CROs and Protein Development teams based in the US and Europe.
• Ensure on time and on quality support to due diligence of China sourced external innovation and business development projects.
• Drives operation excellence and innovation to deliver all tasks with increasing speed and operation efficiency.
• Drive change management and shape a winning culture.
• Develop, coach and engage talents, and ensure diverse bench strength for the future.
• Engage and contribute to the overall Protein Development strategy and deliverables as a member of the Protein Development leadership team
Major Duties & Responsibilities
In order of importance, briefly describe, in sentence form, the essential functions/major responsibilities of this position (principal duties and responsibilities of the position) as it exists today. Describe the job, not the person in the job. Each item listed below should be an essential function/major responsibility of the position, not a day-to-day activity.
Typically, job descriptions should contain no more than seven or eight major responsibilities ranked in order of highest percentage of time to least.
Approximate Percentage of Time Tasks/Duties/Responsibilities
50% Support product launch and ongoing commercial operation in China
20% Engage Chinese health authorities, influence Chinese regulatory policies, and shape Chinese filing strategies
10% Management of headcounts and budgets related to functional activities
10% Member of the Protein Development leadership team and contributes to Protein Development’s strategic and long-range planning
10% Participate various J&J Chinese leadership committees and forums
Required Minimum Education: Master’s Preferred Minimum Education: PhD
Required Years of Related Experience: >15 years’ experience in Biopharmaceutical Development with demonstrated success in engaging Chinese health authorities and shaping Chinese health regulatory policies. Extensive experience of working with China based CDMOs and CROs.
Required Knowledge, Skills and Abilities: Fluent in English and Chinese
Percentage Traveled: 30% Domestic (China) and International
Required Years of People Management Experience: >10 years
Preferred Area of Study: Biochemistry, Biochemical Engineering or relevant disciplines
Preferred Related Industry Experience: Pharma or Biotech
Preferred Knowledge, Skills and Abilities: Experience working with international teams
Key Working Relationships
Internal
IMSC, RA, QA, Commercial Operation, and API, DPDD, and AD within Protein Development
External
Chinese Health authorities, Contractors, CDMO, and CRO,
Required Skills:
Preferred Skills:
Biochemical Engineering, Chemical Engineering, Critical Thinking, Developing Others, Disruptive Innovations, Efficiency Analysis, Financial Competence, Global Market, Inclusive Leadership, Leadership, Performance Measurement, Process Chemistry, Process Optimization, Product Improvements, Quality Assurance (QA), Research and Development, Researching, SAP Product Lifecycle ManagementPlease let Johnson & Johnson Innovative Medicine know you found this job on InterviewPal. This helps us grow!
We scan and aggregate real interview questions reported by candidates across thousands of companies. This role already has a tailored question set waiting for you.
Generate a resume, cover letter, or prepare with our AI mock interviewer tailored to this job's requirements.