Director, Regulatory Affairs

Posted 2 Hours Ago
Be an Early Applicant
Hiring Remotely in Yuzhuang, Beijing, CHN
Remote
Expert/Leader
Biotech • Pharmaceutical
The Role
Lead regulatory strategy and execution for a therapeutic area in China, manage product lifecycle and approvals, engage with regulators and stakeholders, build and lead a regulatory team, ensure compliance with SOPs and good regulatory practices, and drive timely high-quality submissions and crisis management.
Summary Generated by Built In

Typical Accountabilities

  • Play a key role in developing the RA strategy of the designed TA, and drive to implement it.

  • Ensure effective RA activities and deliverable including gaining in-time and high-quality approval and facilitate full speed launch.

  • Maintain product licenses in assigned portfolio through timely lifecycle management with a high standard.

  • Maintain the awareness of market intelligence and shape the regulatory environment relevant to the assigned portfolio.

  • Actively maintain and develop excellent relationship with local regulatory authorities and external stakeholders.

  • To build and retain effective regulatory team, provide leadership and direction to team; maintain cross-functional communication.

  • Adherence to AZ and industry code of conduct, ethics and good regulatory practices (GRP) including AZC RA SOPs and other required SOPs, to drive issue management.

Education, Qualifications, Skills and Experience

Essential

Academic / Professional Qualification

  • Bachelor degree or above in Pharmacy, Medical, Biology or related field.

Technical / Skills Training

  • Have a proven track record on performance and reputation from leading pharmaceutical companies.

  • Fully understand the current regulatory practices and regulation in China.

  • Good networking with regulatory authorities.

  • Strong ability on team management.

  • Strong collaboration across teams.

  • Excellent project management skill and experience.

  • Excellent verbal and written communication skills and fluent in both oral and written English.

  • Able to work with a keen sense of urgency and priority, task oriented with a “Big Picture” approach.

Working Experience

  • Minimum 3 years in leading RA TA with successful delivery track record of RA.

  • Minimum 15 years in leading MNC as regulatory profession and qualified competence. 

  • Rich Experience in handling complex regulatory projects, various kinds of regulatory submissions/approvals.

  • Rich Experience in complex regulatory environment assessment.

  • Rich Experience in crisis management.

Date Posted

15-7月-2026

Closing Date

30-7月-2026

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

Skills Required

  • Bachelor degree or above in Pharmacy, Medical, Biology or related field
  • Proven track record from leading pharmaceutical companies
  • Full understanding of current regulatory practices and regulation in China
  • Good networking with regulatory authorities
  • Strong ability in team management
  • Strong collaboration across teams
  • Excellent project management skill and experience
  • Excellent verbal and written communication skills; fluent in oral and written English
  • Able to work with a keen sense of urgency and priority; task oriented with a "Big Picture" approach
  • Minimum 3 years leading RA therapeutic area with successful delivery track record
  • Minimum 15 years in multinational companies as regulatory professional with demonstrated competence
  • Rich experience handling complex regulatory projects and various regulatory submissions/approvals
  • Rich experience in complex regulatory environment assessment
  • Rich experience in crisis management

AstraZeneca Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AstraZeneca and has not been reviewed or approved by AstraZeneca.

  • Fair & Transparent Compensation Pay is considered competitive across many roles when total rewards are factored in. Senior scientific and leadership bands are described with high ranges that reinforce competitiveness at upper levels.
  • Strong & Reliable Incentives Bonuses, equity eligibility in many salaried roles, and solid sales on‑target earnings with upside are emphasized as meaningful parts of compensation. These elements boost overall value even where base pay is not the very highest.
  • Retirement Support A 401(k) program with a strong company match and immediate vesting is repeatedly cited as a standout. Generous retirement support is viewed as enhancing the total package relative to peers.

AstraZeneca Insights

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The Company
HQ: Gaithersburg, MD
70,000 Employees
Year Founded: 1999

What We Do

We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet.

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