4 jobs found in Sunnyvale

BBG Ventures, LLC is seeking a Compliance Specialist on a hybrid basis in Sunnyvale, CA. The specialist will coordinate activities related to the field action process, support regulatory compliance, and manage documentation. Candidates should hold a bachelor's degree in a relevant field and have over 4 years of experience in product quality or a regulated industry. Familiarity with U.S. medical device regulations and strong communication skills are essential. Contractor benefits include medical, dental, and 401k. #J-18808-Ljbffr

A leading health technology company is seeking a Quality Assurance professional in Sunnyvale, CA. The role involves managing customer complaints, leading CAPA investigations, and supporting the quality management system. Candidates should have a bachelor's degree in a relevant field and at least 2 years of quality assurance experience in the medical device sector. The company offers a competitive salary range of $71,000 - $85,000 and various benefits including healthcare and paid time off. #J-18808-Ljbffr

The Mom Project is seeking a Compliance Specialist on a contract basis in Sunnyvale, CA. This hybrid role requires coordinating field action activities, processing customer acknowledgment forms, and ensuring compliance with regulatory standards. Candidates should possess a Bachelor's degree in a relevant field and at least 4 years of experience in quality or regulatory roles. Key benefits include medical, dental, vision, and 401k options through a third-party employer of record. #J-18808-Ljbffr

Associate Director, Medical Writing (Hybrid - SF Bay Area) We are seeking an experienced Associate Director of Medical Writing to lead the development of high-quality clinical and regulatory documents in support of complex drug development programs. This individual will play a key role in shaping document strategy, ensuring scientific accuracy, and driving cross-functional alignment across clinical, regulatory, and biostatistics teams. This is a hybrid role based in the San Francisco Bay Area . Relocation package is available. Key Responsibilities Lead the planning, authoring, and review of clinical and regulatory documents, including clinical study reports (CSRs), protocols, investigator brochures (IBs), and submission documents Serve as the medical writing lead on complex, multi-phase programs, including late-stage development and regulatory submissions Collaborate cross-functionally with Clinical Development, Regulatory Affairs, Biostatistics, and Clinical...