Senior Regulatory Affairs Specialist Jobs in Lakeside, CA

Empower our regulatory function by leading global strategies for IVD and NGS products, enhancing market authorization initiatives and ensuring compliance throughout product lifecycles while collaborat...

Partner with us to innovate and transform Quality & Regulatory operations through technology and data analytics. Drive automation, improve efficiency, and foster effective digital solutions that enhan...

Unlock potential by navigating complex regulatory landscapes, ensuring compliance for medical devices globally. Collaborate with cross-functional teams to develop strategies that drive product registr...

Join a team that drives regulatory excellence for clinical development, ensuring strategic and compliant submissions. Collaborate cross-functionally to accelerate drug approval processes while oversee...

Partner with us to lead global regulatory labeling strategies, ensuring compliance and accuracy. Collaborate with cross-functional teams throughout the product lifecycle, shaping compelling and compli...

Drive global labeling strategies across product lifecycles, ensuring compliance and alignment with regulatory requirements. Lead cross-functional teams in the development and implementation of accurat...

Transform the quality landscape as a key contributor to our QA team! Drive improvements in GMP documentation, lead audits, and enhance quality systems. Collaborate cross-functionally to elevate compli...

Champion regulatory excellence by overseeing compliance and managing the Regulatory Affairs team. Drive strategies for clinical operations while ensuring adherence to FDA guidelines and GCP standards...

Lead the charge in managing labeling projects for GSS product portfolios. Collaborate across teams to ensure compliance, accuracy, and clarity in product labeling and documentation while enhancing pro...

Accelerate clinical trial success by optimizing monitoring strategies and processes for efficient, quality data management in alignment with regulatory standards and timelines...

Engage in quality assurance for GMP manufacturing while collaborating with cross-functional teams. Take ownership of quality records, ensuring compliance and promoting continuous improvement for new a...

Join a team that's shaping the future of global regulatory strategy. Your expertise will drive compliance, oversee submissions, and lead a dynamic regulatory team in executing key strategies for produ...

Take ownership of regulatory affairs operations, leading teams to enhance processes within clinical trials while ensuring compliance with regulations and fostering collaboration across departments...

Champion the administration and optimization of laboratory systems, ensuring seamless deployment, validation, and integration of informatics solutions within a GMP environment to enhance data integrit...

Manage clinical studies to ensure compliance with regulations and human subject protection. Coordinate site monitoring and maintain quality standards while communicating effectively with site teams to...

Deliver end-to-end bioprocess solutions by leveraging deep expertise in biopharmaceutical workflows, guiding complex customer collaborations, and driving high-impact project leadership for long-term s...

Elevate your career by leading medical education and promotional material reviews, ensuring compliance with FDA regulations while driving strategic direction and process improvements in a collaborativ...

Join a team that's advancing nuclear engineering through component qualification, structural analysis, and seismic qualification for new and existing facilities. Collaborate with multidisciplinary exp...

Transform global regulatory processes by leading approvals, strategizing submissions, and ensuring compliance for medical devices across diverse markets while collaborating with teams and serving as a...

Manage global regulatory strategies for clinical and commercial product registrations. Ensure compliance and successful market access for the PSMA franchise. Lead cross-functional collaborations and d...

Drive impactful marketing campaigns through creative oversight and strategic management. Collaborate with cross-functional teams to enhance digital initiatives, optimize performance, and support organ...

Partner with us to enhance risk management practices for medical devices and diagnostics. This role drives interdisciplinary collaboration to ensure regulatory compliance and product safety across all...

Contribute to lead risk-based quality management for oncology trials across phases. Collaborate with cross-functional teams to assess risk, ensure data quality, and drive mitigation. Provide expert gu...

Reimagine quality assurance by leading teams to enhance compliance, drive product quality, and streamline regulatory processes. Collaborate across functions to implement effective Quality Management S...

Elevate your career by contributing to the validation of critical bioprocess systems. You'll lead a team while ensuring compliance with industry standards and collaborating across departments to drive...