About this opportunity
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
Your Role：
In this pivotal role, you will lead the development and execution of regulatory strategies for new product registrations in China, driving approvals that directly advance patient access to innovative therapies. You will own the end-to-end regulatory submission process, from clinical trial applications through to product approval, ensuring the highest quality of filing dossiers and full alignment with both local and global regulatory requirements.
You will establish and maintain the processes and infrastructure needed to monitor regulatory review timelines, coordinate responses to authority queries, and ensure strategic objectives are delivered on schedule. Acting as the primary interface between the China regulatory team and Global Regulatory Therapeutic Area functions, you will negotiate directly with regulatory authorities on product labeling to secure optimal outcomes for the Chinese market.
Beyond new product registrations, you will manage license renewals and variations for marketed products, supporting the full product lifecycle in line with business objectives. You will contribute to the continuous improvement of regulatory systems, standard operating procedures, and working practices, and ensure all activities are conducted in compliance with applicable policies and standards.
Who You Are：
• You hold a degree in a Life Science or related discipline, with a higher qualification such as a Master's degree or PhD.
• You bring a minimum of 10 years of regulatory affairs experience in the pharmaceutical or biotechnology industry.
• You have an excellent understanding of Chinese regulatory regulations, guidelines, and submission requirements.
• You have a proven track record of preparing and managing regulatory submissions and successfully achieving product approvals.
• You have demonstrated experience engaging and negotiating with regulatory authorities, including the National Medical Products Administration (NMPA).
• You communicate fluently in English, both written and spoken, and are able to collaborate effectively with global and local stakeholders
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
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 544 comparable Regulatory Affairs roles across 109 biopharma companies.
Salary context
127 of 544 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 544 comparable roles
+ 44 more countries
Seniority mix
429 of 544 peers have a known seniority level
Therapeutic area mix
53 of 544 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Notify me about similar jobs
Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
Or follow a whole field: get every new Regulatory Affairs job in China, and choose locations and companies.
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.