Job Scope and Quality Impact:

This position is responsible for providing guidance on regulatory requirements and supporting in global regulatory related projects and tasks ensuring compliance with international regulations, ISO standards, and other regulatory agencies. 海外注冊(cè)

General Description and Duties:

To perform this job successfully, an individual must be able to perform each essential job task satisfactorily. The tasks listed below are representative of the knowledge, skill, and/or ability required. 海外注冊(cè)

ü Provides guidance on regulatory requirements necessary for strategic and contingency planning, including developing regulatory strategic plans to
teams for solutions.

ü Represents regulatory affairs on product development and commercialization teams.

ü Ensures compliance with standards and execution of corrective actions and is the liaison with domestic and international customers and vendors.

ü Develop the global regulatory strategy for the company’s medical devices.

ü Prepares and oversees documentation packages for submission to global regulatory agencies. Tracks timelines and documents milestone
achievements for inclusion in regulatory submissions. Interacts with regulatory agencies as part of submission review and on-site audit support (e.g.,registration documents, and CE marking design dossiers and technical files).

ü Assists with customer complaints/CAPA system.

ü Develops risk assessment review process for all marketed devices and
implementation of changes to risk management process as needed.

ü Monitors proposed and current international regulations and guidance and
advises on the impact of such regulations.

ü Reviews documents for regulatory claims, promotional material, labeling content, product and process changes, and product documentation.

ü Collaborates and takes direction from RA management. Projects and
Other Duties:

ü Perform other duties as assigned.

Position Qualifications

ü Strong working knowledge of international regulations and internal regulations that affect Class III medical devices.

ü Experience working on cross functional projects.

ü Fluent English with strong written and verbal communication skills.

ü Excellent analytical thinking and problem-solving skills.

ü Ability to communicate effectively to team and key stakeholders and present technical information to non-technical partners in a clear and concise way

ü Ability to work effectively in a multiple cultural environment;

Minimum Education:

ü Bachelor’s degree in a related field, a life sciences degree is preferred.

Minimum Experience:

3 years of experience in a regulatory role or related area.