Regulatory Affairs Specialist Jobs in San Diego, CA

Contribute to strategic regulatory submissions and enhance oncology product development. Collaborate with cross-functional teams to ensure compliance, manage timelines, and communicate effectively whi...

Grow your career with strategic quality leadership in medical device development. You'll mentor engineers and integrate quality strategies to ensure our innovative robotic systems are safe, effective...

Contribute to compliance excellence in IVD product development by ensuring all regulatory requirements are met. Work collaboratively with teams to uphold quality standards throughout the entire lifecy...

Drive global regulatory strategies for Phase 2/3 clinical programs, ensuring alignment with health authority requirements. Collaborate across functions to navigate complex regulatory landscapes and le...

Empower your career by leading global regulatory strategies for late-stage clinical programs, ensuring compliance and driving interaction with health authorities to achieve successful product commerci...

Pioneer regulatory excellence by leading FDA submissions and compliance. Manage the lifecycle of medical product filings, ensuring alignment with evolving regulations across diverse jurisdictions in a...

Execute R&D and Regulatory IT projects, ensuring compliance and timely delivery while leading cross-functional teams and managing system enhancements for optimal performance within budget constraints...

Deliver impactful CMC regulatory support for IND/CTA development and maintenance, ensuring compliance and completeness across submissions while leading cross-functional collaboration and strategically...

Unlock potential by leading CMC regulatory activities for IND/CTA development. Drive compliance and quality in submissions, assess CMC changes, and collaborate cross-functionally to support clinical t...

Optimize CMC regulatory strategies for biologic products across the product lifecycle. Lead cross-functional teams to ensure compliance with global regulatory standards while driving successful submis...

Join a team that's driving global regulatory compliance and product stewardship initiatives, ensuring alignment with commercial strategies and effective management of risks to support business growth...

Champion quality assurance excellence in GMP for drug substance and products, overseeing compliance and methodologies. Collaborate to ensure regulatory adherence while maintaining operational efficien...

Champion regulatory excellence by leading compliance initiatives and submission strategies for in vitro diagnostics, ensuring adherence to U.S. and European regulations while partnering with cross-fun...

Join a team that's dedicated to excellence in Quality Control activities, ensuring compliance and accuracy in complex research submissions. Collaborate with leadership to enhance workflow and drive co...

Champion the validation of biopharma systems, leading teams to ensure compliance and excellence in commissioning, qualification, and project management while fostering a collaborative team environment...

Join us to enhance operational excellence by providing quality oversight and support in manufacturing processes. Collaborate with diverse teams to drive improvements and ensure compliance throughout b...

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...

Take ownership of regulatory and medical writing initiatives, leading the creation of complex clinical documents for global submissions. Collaborate with cross-functional teams to ensure compliance an...

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...

Architect enterprise-level Direct Materials Certification strategies, ensuring compliance and driving modernization. Influence stakeholders to solve regulatory challenges and enhance supply chain flex...

Shape the future of healthcare compliance by executing data-driven monitoring and analytics. Develop actionable frameworks and dashboards to ensure oversight and enhance operational effectiveness in a...

Lead the charge in shaping regulatory strategy for innovative medical devices. As the key regulatory authority, oversee submissions, compliance, and cross-functional collaboration to drive the success...

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...

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...

Advance regulatory strategies and submissions for development programs, ensuring compliance with local and global standards. Collaborate on cross-functional teams and lead regulatory processes to achi...