Senior Regulatory Affairs Specialist Jobs in Thousand Oaks, CA

Elevate your career by leading compliance and quality in clinical trials. Collaborate with teams to ensure protocol adherence, site training, and resolve issues while maintaining high standards of mon...

Tackle clinical monitoring challenges while leading site initiatives for quality compliance and protocol adherence. Collaborate with cross-functional teams to ensure successful clinical trial executio...

Optimize your clinical research career by playing a vital role in overseeing and conducting site monitoring for clinical trials, ensuring compliance, quality, and effective team collaboration througho...

Unlock potential by leading site monitoring for clinical trials. Collaborate closely with cross-functional teams to ensure compliance, enhance recruitment, and oversee execution while providing guidan...

Join a team that's driving compliance excellence in supply chain operations. This role blends collaboration across Contracts, Legal, and Supply Chain, focusing on government contracting and ensuring r...

Join a team that's dedicated to enhancing clinical trial quality through leadership, mentorship, and oversight. Engage remotely with cross-functional teams, driving high standards for patient safety a...

Join a team that's dedicated to advancing medical device regulations. Drive compliance through documentation, submissions, and market entry strategies while engaging with cross-functional teams in a d...

Manage reimbursement strategies supporting business goals across product areas. Collaborate with teams to guide product development, analyze landscapes, and educate stakeholders on reimbursement impac...

Join a team that's dedicated to ensuring dietary supplement quality by executing robust QA GMP compliance processes. Your expertise will be pivotal in managing supplier quality and driving continuous...

Unlock potential by leading reliability engineering initiatives to enhance the performance, availability, and lifecycle of critical facility systems across research environments, ensuring operational...

Champion compliance initiatives by conducting research, analyzing trends, and collaborating with teams to ensure accurate and effective regulatory responses. Leverage data-driven insights to support c...

Partner with us to manage critical project agreements, ensuring compliance and facilitating collaboration across teams for effective contract execution and risk assessment in a dynamic biopharma envir...

Explore opportunities as a Clinical & Regulatory Information Management SME, supporting client delivery across VeevaRIM and Clinical initiatives. Engage with stakeholders, optimize processes, and enha...

Join our mission to cure cancer by providing Quality Engineering oversight of validated computer systems, ensuring compliance with regulations while fostering collaboration and driving risk-based deci...

Join a team that's committed to operational excellence through leadership of the Enterprise Quality Audit team, driving compliance, continuous improvement, and quality governance across business units...

Lead the charge in compliance strategy for U.S. Commercial and Market Access. Collaborate with senior leaders to guide complex compliance issues, manage risks, and support innovative business objectiv...

Drive effective quality assurance by conducting advanced audits to ensure compliance with cGMP and regulatory standards globally. Collaborate with management to address compliance issues in complex ma...

Oversee promotional material reviews and ensure regulatory compliance in the pharmaceutical sector. Collaborate with cross-functional teams to align business objectives with FDA regulations, driving i...

Deliver high-quality clinical monitoring in a fast-paced environment. Lead site management, ensure adherence to protocols, and guarantee participant safety. Collaborate effectively while adapting to c...

Engage as a key player in driving regulatory compliance for domestic cloud seeding programs. Lead the scoping of requirements, manage permit submissions, and ensure timely authorization while building...

Pioneer innovative upstream bioprocess solutions by collaborating with biopharma clients and leading technical projects focused on cell culture, media prep, and automation. Drive engineering excellenc...

Join a dedicated team as you lead technical investigations in complaints, leveraging data analytics and root cause methodologies to drive product improvements and enhance patient experience. Engage cr...

Transform proposal development by leading cross-functional teams to deliver compelling bids that showcase innovative solutions. Manage proposals from conception to submission, ensuring clarity, accura...

Join as a Clinical Research Associate to oversee critical monitoring tasks across diverse clinical studies. Ensure high-quality standards while facilitating communication between project teams and sit...

Take ownership of safety analysis deliverables, ensuring high quality and timely execution while leading cross-disciplinary collaboration to support the Mark 1 reactor's licensing and design phases...