Senior Regulatory Affairs Specialist Jobs in San Diego, 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...

Grow your career with a dynamic team managing regulatory projects for IVD devices. Engage in global compliance, product development, and ensure adherence to medical device regulations. Collaborate wit...

Provide regulatory expertise by preparing submissions, ensuring compliance, and collaborating with teams to maintain quality guidelines, supporting product development efforts and compliance with glob...

Lead the charge in regulatory efforts for software solutions, ensuring compliance with FDA and international standards while collaborating with cross-functional teams to drive innovation and streamlin...

Invent innovative clinical regulatory strategies for next-gen diabetes devices, collaborating globally across various teams to navigate complex regulations and ensure successful product submissions in...

Elevate compliance and risk management in FDA-regulated clinical research through expert leadership and quality oversight across clinical trials, ensuring effective protocols and inspection readiness...

Lead the charge in global regulatory strategies for innovative medical devices, driving project success from registration to compliance. Collaborate across teams to enhance healthcare technologies and...

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...

Unlock potential by coordinating regulatory submissions for product approvals, ensuring compliance with regulations and company policies. Drive project timelines, participate in internal strategies, a...

Join a team that's dedicated to advancing regulatory strategies for innovative SaMD products. Collaborate cross-functionally to drive compliance, manage documentation, and ensure readiness for audits...

Drive regulatory excellence by managing submissions, guiding teams, and ensuring compliance. Utilize your expertise to support global projects and foster collaboration in a fast-paced environment focu...

Reimagine global compliance strategies as you guide regulatory submissions, assess product impacts, and collaborate across teams to ensure adherence to medical device regulations while enhancing quali...

Drive global regulatory labeling initiatives, ensuring compliance and quality of documentation across diverse markets. Lead strategic governance, influence policies, and collaborate cross-functionally...

Engage with a dynamic team to facilitate regulatory operations for novel therapeutics. Drive submissions to FDA/CVM while collaborating across multidisciplinary teams to set new regulatory standards i...

Engage in regulatory strategy development and submissions for software products across global markets. Collaborate with cross-functional teams to ensure compliance and approve documentation for innova...

Innovate robust global regulatory frameworks to enhance compliance, drive quality initiatives, and support strategic goals across diverse teams while ensuring adherence to international standards and...

Unlock potential by leading regulatory CMC strategies for oncology products, coordinating submissions, and collaborating across teams to ensure compliance and successful product registration in a dyna...

Drive regulatory strategy by collaborating cross-functionally to influence promotional activities, ensuring compliance while optimizing risk management for impactful business decisions across a dedica...

Join a team dedicated to ensuring drug quality compliance by performing data integrity audits, assessing adherence to FDA standards, and providing actionable recommendations to enhance regulatory deci...

Drive regulatory excellence in the development and lifecycle of IVD medical devices. Collaborate with cross-functional teams to navigate FDA submissions and maintain compliance throughout the product...

Lead the charge in shaping global CMC regulatory strategies, ensuring quality submissions, and driving compliance across development programs while collaborating with cross-functional teams and health...

Advance your career by leading CMC regulatory strategy for small molecule products, ensuring compliance across development and commercialization. Collaborate with cross-functional teams to align objec...

Grow your expertise in CMC Regulatory Affairs, leading strategic initiatives for small molecule drug products from development through commercialization. Collaborate cross-functionally to align regula...

Join our team to lead regulatory strategies across major programs, driving impactful submissions and fostering collaboration within a challenging and dynamic environment. Embrace the opportunity to in...

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...