Senior Regulatory Affairs Specialist Jobs in Lakeside, CA

Join a dynamic team to provide comprehensive regulatory support across clinical, submission, and post-approval phases for pharmaceutical products, ensuring compliance with global regulations while man...

Join a team that's dedicated to ensuring regulatory compliance for medical devices. Lead initiatives for domestic and international registrations while collaborating with marketing and development tea...

Transform medical device regulatory processes by collaborating across teams to ensure compliance and facilitate submissions for both domestic and international markets, while safeguarding product qual...

Empower global labeling excellence by managing regulatory compliance, overseeing document governance, and collaborating with cross-functional teams to ensure safe and effective use of innovative medic...

Lead the charge in ensuring compliance with global regulatory standards, facilitating efficient processes for product registration. Collaborate cross-functionally while managing submissions and develo...

Unlock potential by leading comprehensive regulatory strategies for complex devices. Act as a key expert in multiple scientific disciplines, managing priorities while ensuring compliance with global r...

Explore your career in regulatory submissions, ensuring compliance and alignment with local and regional requirements. Play a key role in the coordination of critical filings, supporting product appro...

Shape global CMC regulatory strategies, lead submissions, engage with stakeholders, and drive compliance for cell therapy products in a fast-paced, collaborative environment, ensuring successful devel...

Bring your expertise to a dynamic role ensuring global regulatory compliance for medical devices. Collaborate across teams to support product development from conception to market, ensuring adherence...

Join a team that's revolutionizing surgical solutions by driving regulatory strategy and approval processes for cutting-edge medical devices. Collaborate with engineering and clinical teams to bring i...

Join a team that's shaping the future of global regulatory affairs. You will lead compliance strategies for investigational products and marketing applications through effective submissions and collab...

Join a dynamic team as you drive regulatory strategies and ensure compliance in post-approval activities for CMC processes. Collaborate cross-functionally, influencing clinical outcomes and advancing...

Champion global regulatory strategies by leading diverse teams in navigating complex approval processes for medical devices. Drive compliance and ensure optimal product launch pathways while addressin...

Transform regulatory operations by leading submission strategies, managing systems, and ensuring compliance across portfolios while collaborating with cross-functional teams for successful outcomes...

Join a team that's dedicated to ensuring compliance in promotional activities for CNS treatments while navigating regulatory pathways in a fast-paced environment. Help shape communications, drive stra...

Optimize regulatory strategies and compliance globally by leading cross-functional projects, guiding teams, and liaising with health authorities throughout the drug development lifecycle to ensure suc...

Join a team that's at the forefront of IVD product compliance and regulatory excellence. Utilize your expertise in 510(k) submissions and navigate the complexities of FDA regulations to drive successf...

Join us to drive quality assurance in GMP/GDP auditing, ensuring compliance and inspection readiness across our partner network. Collaborate with cross-functional teams to enhance supplier qualificati...

Join a dynamic team focused on executing GMP/GDP audits and ensuring compliance across suppliers. Collaborate with cross-functional partners to maintain high-quality standards and drive continuous imp...

Drive regulatory strategies and oversee compliance for investigational therapies. Work cross-functionally to ensure timely regulatory filings and maintain vendor relationships, contributing to clinica...

Shape the future of regulatory strategies through project leadership, ensuring compliance and optimizing processes in collaboration with cross-functional teams and regulatory authorities for successfu...

Shape the future of medical devices by leading regulatory strategies, ensuring compliance across global markets, and mentoring a dedicated team. Empower innovation through effective communication with...

Lead regulatory compliance programs ensuring inspection readiness and proactive risk management across cross-functional teams. Monitor compliance health, manage data quality, and drive improvements al...

Advance regulatory strategy and submissions for CMC in pharmaceuticals, collaborating with cross-functional teams to ensure compliance with FDA, EMA, and ICH standards while overseeing product lifecyc...

Unlock potential by leading quality oversight in medical device development, ensuring compliance with industry standards, and driving risk management strategies for successful product launches and con...