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Regulatory Affairs Specialist Manager At ARC Medical Devices Inc.

Location: Vancouver, British Columbia

Job Description

Mission

The mission of the Regulatory Affairs Specialist Manager is to work with our VP Reg & QA to design and execute ARC's regulatory strategy to maximize market access for ARC's medical devices for the reduction of post-surgical adhesions.

You

Who or What is ARC Medical Devices Inc.?

ARC is developing and commercializing novel, first-in-class solutions to prevent post-surgical adhesions - which if not prevented cause pain & suffering, organ dysfunction, infertility, and death; and for which there is a dire unmet medical need.

Our products are non-viscous, liquid, polysaccharide-based medical devices. Our preclinical data in numerous surgical adhesion models show that our product flows throughout the entire surgical site and reduces the formation of surgical adhesions throughout the entire surgical site. We've recently built a manufacturing facility & QA laboratory; and are implementing our quality management system now. We will initiate first-in-human and follow-on clinical trials in the near-term.

We

Outcomes

Why Work at ARC Medical Devices Inc.?

Required Designations & Experience

Competencies - Role Specific

Competencies - Culture Fit

Equal Opportunity Employer

We are an equal opportunity employer and evaluate applicants without regard to race, colour, national origin, religion, gender, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law.

Travel Requirements

We anticipate that approximately 25% of the time for this position may include international travel.

Location

We are in Richmond, British Columbia, Canada - right beside Vancouver. From our facilities to the Vancouver International Airport is about a 10-minute drive; and to the heart of downtown Vancouver is about a 30-minute drive.

How To Apply

Job Type: Full-time

Experience:

Education:

Language: