Medella Life Jobs in United States

The Senior Clinical Project Manager (Sr. CPM) provides strategic and operational leadership for complex clinical trials across multiple phases. · This role is accountable for study delivery, financial oversight, cross-functional leadership, and sponsor relationship management, · ...

We are seeking a Senior Regulatory & Quality Senior Manager to lead client's regulatory affairs and quality management efforts. · ...

We are seeking a hands-on Director of Regulatory Affairs to lead global regulatory strategy for a Class II medical device company. This role will own 510(k) strategy, agency engagement, and submission execution in a growing, innovation-driven company. Their portfolio consists pri ...

We are supporting a small medical device company in New York in the search for an experienced Senior Regulatory & Quality Manager. · The company develops complicated medical devices currently marketed as Software as a Medical Device (SaMD). · This Hybrid position combines senior ...

Job summary · Regulatory Affairs Manager for medical devices company. · Partner closely with the Director of Regulatory Affairs to define and implement regulatory strategies. · Provide regulatory guidance during product development to ensure compliance. · ...

About the Role · We're looking for a Quality Director to lead and evolve our quality function as we scale regulated medical devices that incorporate AI/ML software. This role sits at the intersection of hardware, software, and data science and will be critical in ensuring our pro ...

We are partnering with a mid-sized medical device company with an established commercial presence and a strong pipeline of next-generation products. · As part of this growth, they are looking to add a Senior Quality Engineer who can operate strategically while remaining hands-on ...

About the Role · We're looking for a Quality Director to lead and evolve our quality function as we scale regulated medical devices that incorporate AI/ML software. This role sits at the intersection of hardware, software, and data science and will be critical in ensuring our pro ...

We are seeking a Senior Director, Regulatory Affairs (CMC) for a California based clinical-stage biotech advancing toward late-stage development and commercialization. This visible leadership role will own global CMC regulatory strategy through NDA/BLA and lifecycle management, p ...

About the Role · We're looking for a Quality Director to lead and evolve our quality function as we scale regulated medical devices that incorporate AI/ML software. This role sits at the intersection of hardware, software, and data science and will be critical in ensuring our pro ...

We are seeking a hands-on · Director of Regulatory Affairs · to lead global regulatory strategy for a Class II medical device company. This role will own 510(k) strategy, agency engagement, and submission execution in a growing, innovation-driven company. Their portfolio consists ...

The Digital Health Strategy role is responsible for defining, developing, · and executing digital health initiatives that improve patient outcomes, · operational efficiency, and business performance.Develop and lead the organization's digital health strategy, · ...

We are supporting a small medical device company in New York in the search for an experienced Senior Regulatory & Quality Manager. · ...

About the Role · We're looking for a Quality Director to lead and evolve our quality function as we scale regulated medical devices that incorporate AI/ML software. This role sits at the intersection of hardware, software, and data science and will be critical in ensuring our pro ...