Top Tech Jobs & Startup Jobs in San Francisco Bay Area, CA

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.

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

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

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

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 medical device projects ensuring compliance with regulations. Collaborate with cross-functional teams for planning, execution, risk management, and reporting.

The Clinical Data Manager oversees the quality and integrity of clinical trial data, ensuring compliance with protocols and regulations while collaborating with various teams.

The role involves providing regulatory guidance, assisting in FDA submissions, conducting assessments, and collaborating with clients and teams to ensure compliance with FDA regulations.

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