Regulatory Affairs / Admin
Regulatory Affairs / Admin
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Roles and Responsibilities:
Supports the Regulatory Affairs team to help them stay organized and complete tasks that allow the team to focus on more advanced responsibilities.skills. Work is generally of a critical or confidential nature.
Creating populating and updating project trackers
Compiling data and preparing reports
Generating updating and archiving regulatory documentation
Organizing meetings (including note taking and distribution of meeting minutes)
Assisting Regulatory Submissions team with ECO creation Product Registration database entry and other processes related to documentation release and archival.
Carrying out administrative tasks in a fast-paced environment with many deadlines at all levels of the organization.
Coordinating activities between departments and outside parties.
Reviewing and updating work instructions and procedures related to regulatory submissions.
Creation of POs and submission of invoice payments for the Regulatory Affairs department.
Required Skills and Experience
Excellent written and verbal communication skills.
Effective time management and organization skills.
Attention to detail and self-motivated
Ability to work with associates with varied skills and levels of experience.
Basic computer skills
Proficient in Microsoft Office (Outlook word excel powerpoint etc.)
Ability to follow through and complete assigned tasks.
Required Education and Training
High school diploma/Secondary Education or equivalent; vocational training with
additional five (5) years of on-the-job training/experience in a related field
OR
Bachelors degree (or equivalent) plus four (4) years of experience
Preferred Skills and Experience
Project Management experience a plus
Experience working with FDA websites
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Employment Type
Full-time
