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The Regulatory Associate will assist in preparing domestic and international regulatory submissions and represent the department in project team meetings. They are responsible for reviewing controlled documents, tracking submission timelines, and ensuring compliance with global health authority regulations.
Purpose and Scope
Under supervision, assist in all functions pertaining to domestic and international regulatory submissions, including preparation of documents for electronic or paper filing for drug projects. This includes working on project teams to guide development to meet regulatory registration requirements.
Essential Duties & Responsibilities
Knowledge, Skills & Abilities
Core Values
This position is expected to operate within the framework of Tolmar’s Core Values:
Education & Experience
Working Conditions
Compensation and Benefits
Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience.
Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors.
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