Abbott Regulatory Affairs Job in Taiwan | Apply Now
An Abbott regulatory affairs job opportunity is available in Taipei, Taiwan for a Regulatory Affairs Specialist. This role is ideal for candidates with a background in Life Sciences or Pharmacy, looking to engage in regulatory submissions and compliance activities.
- Position: Regulatory Affairs Specialist
- Location: Taipei, Taiwan
- Category: Regulatory Affairs
About Abbott
Abbott is a global healthcare company that develops and delivers a range of innovative products and services in the fields of nutrition, diagnostics, medical devices, and pharmaceuticals. With a commitment to improving the health of people around the world, Abbott operates in more than 160 countries, providing access to high-quality healthcare solutions.
Abbott regulatory affairs job Description
The Abbott regulatory affairs job involves preparing, submitting, and obtaining approvals for medical device registrations and other regulatory permits for assigned products in Taiwan. The role involves supporting post-approval regulatory activities and ensuring ongoing compliance with regulatory requirements.
Eligibility Criteria
- Bachelor’s degree or higher required, preferably in Life Sciences, or a related field.
- Good interpersonal and communication skills.
- Sufficient English communication skills, including reading, writing, listening, and speaking, to perform job responsibilities effectively.
- Adaptable to complex work environments and tasks.
- Familiar with the use of Microsoft Office.
Abbott regulatory affairs job – Key Responsibilities
- Prepare, submit, and obtain approvals for medical device registrations and other regulatory permits for assigned products in Taiwan, while supporting post-approval regulatory activities and ongoing compliance requirements.
- Coordinate with Corporate Regulatory Affairs, Subject Matter Experts (SMEs), regulatory agencies, and internal cross-functional stakeholders to support regulatory submissions, compliance activities, and business objectives.
- Maintain accurate, organized, and audit-ready regulatory documentation, quality records, registration plans, and related materials using company systems and tools (e.g., WindChill).
- Evaluate product changes and applicable regulatory requirements throughout the product life cycle and support the implementation of necessary actions to ensure continued regulatory compliance.
- Complete all assigned training and provide regulatory, administrative, and operational support to the direct supervisor and Regulatory Affairs team in accordance with company policies, procedures, and quality system requirements.
- Perform administrative tasks related to the department as required by the line manager.
- Perform additional tasks assigned by the line manager when required.
- Execute job responsibilities in accordance with applicable Standard Operating Procedures (SOPs) under Global Regulatory Services.
This Abbott regulatory affairs job is an excellent fit for qualified candidates looking to make an impact in the regulatory field. Interested individuals are encouraged to apply at the earliest before the deadline.
