Senior Regulatory Science Specialist (1 year Fixed Term)

Other US Location Posted Jan 20, 2025 0 views

Compensation

Compensation not disclosed

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Job description

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
#LI-PFE

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