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Join a roster of clinical specialists to provide insights on medical devices during regulatory assessments, on an as-needed basis. Short engagements ensure certified devices meet clinical performance standards.

The Active Device Specialist will assess technical documentation, establish internal processes for active medical devices, and incorporate relevant standards for assessments.

As a Software Safety Engineer, you will assess medical devices' software, support regulatory insights, collaborate with teams, and improve systems.

The Commercial Relations Manager will build relationships with third parties in the digital health sector, ensuring they understand Scarlet's value and advocate for the company. Responsibilities include networking, collaborating with teams, and attending industry events to enhance awareness and commercial goals.

The role involves building commercial relationships with regulatory consultants and industry stakeholders in the US digital health industry, enhancing Scarlet's presence in the market. Responsibilities include networking, knowledge sharing, attending events, and collaborating with the Commercial team to achieve goals.

The Business Development Representative will prospect and qualify leads, build a pipeline of prospects, manage qualification conversations, and collaborate with the commercial team to refine strategies.

Conduct remote audits of medical device manufacturers' Quality Management Systems under regulatory standards, ensuring compliance and high-quality audit experiences.

Scarlet seeks passionate individuals motivated by healthcare innovation to enhance software and AI integration in healthcare markets. Ideal candidates are curious, innovative, and possess strong communication skills. Experience in HealthTech is a plus.

The Account Executive is responsible for building relationships with decision-makers in healthcare technology, managing the sales motion from discovery to closure, and improving sales processes while collaborating with team members.

The role involves creating content and training materials related to Quality Management Systems for medical devices, focusing on regulatory compliance and audit preparation.