Roles and Responsibilities:
- Manages cross-functional projects to establish processes or process improvements.
- Manage departmental projects, as requested.
- Formulates and gains approval for project plans.
Qualifications:
- 7+ years of experience leading and executing the coordination of projects in the medical device or pharmaceutical industry.
- Experience with medical device development and design control is required.
- Demonstrated understanding of FDA Quality System Regulation (21 CFR 820), ISO 13485, and EU Medical Device Regulation.
Cognito Therapeutics
Cognito Therapeutics, Inc. translates scientific findings from MIT into therapeutic approaches for brain health, including Alzheimer’s disease and other neurodegenerative conditions. They are a fast-moving, highly motivated team of innovators with the ambitious goal of helping millions of patients and caregivers around the world.