Senior Regulatory Science Specialist (1 year Fixed Term)

Posted 3 Days Ago
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Seoul
Hybrid
Mid level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
The Senior Regulatory Science Specialist will prepare and submit filings for new drug marketing approvals, ensure compliance with local regulations, and maintain product documentation. They will also coordinate activities among various divisions, provide regulatory information, and establish relationships with regulatory authorities.
Summary Generated by Built In

Job Responsibility

  • Prepares filings and obtains marketing approval from the MFDS for a planned new drug (K-NDA) and ensures subsequent maintenance of drugs registered (Supplemental & Amended K-NDA).
  • Ensures quality filings of K-IND submission and its approval.
  • Updates the assigned Local Product Documents (LPDs) in consistent with the local regulations and CDS update, and ensures timely updates for the related systems (e.g. PEARL, GDMS, and etc.).
  • Provides regulatory science related information to other divisions/departments.
  • Is aware of the external regulatory environment, including competitor intelligence and regulatory actions, in order to provide informed input to regulatory strategies.
  • Coordinates regulatory activities between divisions/departments (Clinical, Medical, Business Units, Corporate Science, Quality Operations, and PRD etc.).
  • Ensures registered products are maintained and updated in full compliance with all relevant legislation and SOPs.
  • Assists Regulatory Science Team Lead. to establish, develop and maintain close working relationships with the relevant regulatory authorities and associations (MFDS, MOHW, KRPIA etc.).
  • Assists Regulatory Science Team Lead for coordinating regulatory activities between Divisions/Business Units and timely communications with PRD etc..
  • Supports and collaborates with Business Groups for related works.


Qualifications

  • Pharmacist (Pharm.D) or Master's degree in a scientific field
  • Minimum 2 years experience in pharmaceutical industry for Bachelor's degree in a scientific field
  • Negotiating, communication and interpersonal skills
  • Working knowledge of computer applications
  • Fluency in written and spoken English


SKILLS

  • Professional Expertise
  • Decision-making/ Judgment
  • Negotiation
  • Leadership
  • Project Management
  • Teamwork


Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Regulatory Affairs
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What the Team is Saying

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The Company
HQ: New York, NY
121,990 Employees
Hybrid Workplace
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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