This job posting has expired
Expired on April 4, 2026
Job Description
Leads/supervises a team of more than 2 professionals within the Regulatory Affairs Sub-Function. First level manager of a work team that may comprise professionals, technical and/or administrative staff.
Main Responsibilities:
- Supervises professionals in directing development of product registration submission, progress reports, supplements, or amendments.
- Interacts with regulatory agency to expedite approval of pending registration.
- Serves as regulatory liaison throughout product lifecycle.
- Advises development and/or marketing teams on manufacturing changes, line extensions, and technical labeling.
Responsibilities
- Supervises development of product registration submissions
- Interacts with regulatory agency to expedite approval
- Serves as regulatory liaison throughout product lifecycle
- Participates in product plan development and implementation
- Ensures timely approval of new drugs, biologics or medical devices
- Advises teams on manufacturing changes and technical labeling
Qualifications
- Associates Degree (± 13 years)
- Minimum 4 years of experience