Regulatory Affairs Specialist Jobs in Santa Clara, CA

Lead the charge in navigating complex regulatory challenges for innovative medical devices, ensuring successful approvals in the US and globally through strategic planning and independent judgment on...

Lead the charge in regulatory project management, driving cross-functional execution and strategies for global drug submissions. Collaborate closely with teams to ensure timely completion of critical...

Optimize regulatory operations by coordinating submissions, ensuring compliance, and collaborating with cross-functional teams. You'll empower the Regulatory Affairs department through effective commu...

Drive quality assurance excellence by overseeing compliance, batch review, and documentation practices, while collaborating with cross-functional teams to enhance operational efficiency and product re...

Champion regulatory excellence in food safety and nutrition, leveraging deep expertise to guide clients through complex compliance challenges and develop impactful strategies for product approvals and...

Unlock impactful regulatory strategies for global development, driving compliance and excellence in early and late-stage clinical programs while collaborating across teams to facilitate product regist...

Engineer quality solutions in the medical device sector. Oversee compliance, drive risk management, and enhance product quality. Collaborate with teams throughout product lifecycle ensuring adherence...

Pioneer clinical excellence by supporting multiple studies, ensuring compliance with regulations, timelines, and SOPs. Collaborate cross-functionally to generate high-quality clinical evidence while m...

Transform global regulatory strategies to meet asset goals and health authority requirements. Collaborate across teams to ensure high-quality submissions and mitigate risks while driving compliance in...

Transform the clinical trial landscape by leading site monitoring efforts, ensuring compliance and quality in study execution, while collaborating with diverse teams to enhance recruitment, training...

Shape the future of clinical trials by enabling top-notch support and coordination for successful project execution. This role involves interaction with clinical sites, ensuring compliance, and mainta...

Drive quality assurance processes ensuring compliance with GMP and cGMP standards. Collaborate with external partners on activities such as batch record review, product release, and quality metrics wh...

Drive regulatory strategy for AI-powered cardiac and pulmonary tools, ensuring compliance and accelerated market access across global markets by leading submissions and fostering cross-functional coll...

Advance your career in regulatory advertising by leading compliance initiatives for promotional materials. Provide strategic guidance across teams, ensuring effective communications that satisfy FDA r...

Elevate client relationships by delivering customized analytical solutions, engaging in dynamic project management, and contributing to innovative materials characterization efforts within a collabora...

Manage key regulatory functions, guiding compliance in PBM, pharmacy, and healthcare technology. Advise on state and federal obligations, and translate regulations into practical strategies for busine...

Deliver Quality Assurance support in a fast-paced CDMO environment. Collaborate across teams to enhance compliance with GMP regulations and QA systems, ensuring robust quality control processes and co...

Drive strategic risk mitigation efforts by analyzing offline threats, enhancing safety protocols, and collaborating with cross-functional teams to protect users from organized crime and other offline...

Engage in leading GCP audit programs, managing staff development, and implementing quality initiatives to enhance safety compliance. Contribute to a dynamic, science-focused environment dedicated to i...

Shape the future of environmental compliance by leading on-site programs, ensuring adherence to regulatory standards, and fostering sustainability initiatives across operations with minimal supervisio...

Analyze and document medical device reports for regulatory compliance, ensuring they meet international standards. Collaborate with cross-functional teams to drive improvements in processes and suppor...

Accelerate progress at our Diabetes Care division by ensuring compliance with medical reporting regulations, documenting medical events, and collaborating with cross-functional teams to enhance produc...

Champion cross-functional collaboration to drive quality assurance practices and enhance product development. Lead Design Assurance initiatives, ensuring compliance with regulatory standards while men...

Drive efficiency in project billing and workflow management by overseeing setup, ensuring data integrity, and facilitating vendor invoice processing in Certinia. Collaborate with finance and project t...

Lead the charge in developing and overseeing global product labeling strategies for Neuromodulation therapies, ensuring compliance with regulatory standards, and fostering cross-functional collaborati...