Top Tech Jobs & Startup Jobs in Denver & Boulder, CO

The EU Generalist manages EU regulatory compliance, advises on product development and submissions, collaborates across teams, and stays updated on regulatory trends.

The Biostatistician designs, analyzes, and interprets clinical trial data, collaborating with various teams and ensuring statistical rigor and compliance with regulatory standards.

The Quality Engineer ensures products comply with medical device regulations, supports design control, conducts risk management, and participates in validation processes, audits, and improvement initiatives.

Provide expert consultation on bioequivalence studies, review protocols, oversee study designs, conduct analyses, and collaborate with teams to ensure compliance and execution of bioequivalence programs.

The Project Manager will lead cross-functional projects in life sciences, develop project plans, manage budgets, and ensure compliance with GxP and FDA regulations.

The UX/UI Designer will create compliant digital experiences for medical devices, leading design processes, collaborating with teams, and conducting user research to validate designs.

Lead GxP consulting engagements, optimize Quality Management Systems, provide compliance guidance, and mentor junior staff in the life sciences industry.

Serve as the primary clinical expert, provide guidance in clinical development, monitor trials, analyze data, and collaborate with teams to ensure compliance and patient safety.

The Contract Administrator will support contract development, review, and negotiation activities in the medical device industry, managing clinical study agreements and vendor contracts while collaborating with various teams to ensure compliance and efficiency.