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ICONMA, LLC Regulatory Program Manager in United States

Key Qualifications: 8+ years of program/project management experience in a regulated industry, preferably in medical products and/or digital health Proven track record of driving regulatory submissions, approvals, and launches with multi-disciplinary teams Outstanding communication and organizational skills. Ability to optimally manage multiple projects simultaneously Excellent analytical and problem-solving capabilities, with a keen eye to detect and mitigate risks Independent self-starter who thrives in ambiguous environments Hands-on experience in the use of project management and reporting software Additional Requirements: Experience with Design Controls and Quality Systems Solid understanding of regulatory process for different classes of medical devices in both the US and internationally Education & Experience: BS/MS in Engineering, Biomedical Science or equivalent science degree. As an equal opportunity employer, ICONMA pride itself on creating an employment environment that supports and encourages the abilities of all persons regardless of race, colour, gender, age, Sexual orientation, citizenship, or disability

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