Posted:
10/5/2025, 10:13:55 AM
Location(s):
Matsudo, Chiba Prefecture, Japan ⋅ Chiba Prefecture, Japan
Experience Level(s):
Mid Level ⋅ Senior
Field(s):
Legal & Compliance
MAIN RESPONSIBILITIES
•
As the Team Leader (Professionals) of the Regulatory Affairs Sub-Function, supervises professionals in directing development of product registration submission, progress reports, supplements, amendments, or periodic experience reports.
•
Interacts with regulatory agency to expedite approval of pending registration.
•
Serves as regulatory liaison throughout product lifecycle.
•
Participates in some of the following: product plan development and implementation, regulatory strategy, risk management, chemistry manufacturing control (CMC).
•
Ensures timely approval of new drugs, biologics or medical devices and continued approval of marketed products.
•
Serves as regulatory representative to marketing, research teams and regulatory agencies.
•
Advises development and/or marketing teams on manufacturing changes, line extensions, technical labeling, appropriate regulations and interpretations.
QUALIFICATIONS
Education
Education Level
Major/Field of Study
Or
Education Level
Associates Degree (± 13 years)
Experience/Background
Experience
Experience Details
Minimum 4 years
Licenses and Certifications
License/Certification
Language Proficiency
Language
Proficiency
Note: This job description is not to be considered an exhaustive statement of duties, responsibilities or requirements and does not limit the assignment of additional duties for this role.
The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.
Website: https://abbott.com/
Headquarter Location: Illinois City, Illinois, United States
Employee Count: 1001-5000
Year Founded: 1944
IPO Status: Public
Last Funding Type: Post-IPO Debt
Industries: Biotechnology ⋅ Emergency Medicine ⋅ Genetics ⋅ Health Care ⋅ Health Diagnostics ⋅ Manufacturing ⋅ Medical ⋅ Medical Device ⋅ Nutrition ⋅ Pharmaceutical