Regulatory Affairs Specialist Jobs in Santa Monica, CA

Lead the charge in ensuring compliance and efficiency in the IVD labeling conversion process while collaborating across departments to maintain project timelines and technical accuracy...

Empower global product registration by managing regulatory submissions, collaborating across teams, and ensuring compliance with market regulations. Lead initiatives that drive strategic growth while...

Seeking a detail-oriented Regulatory Affairs Specialist to manage medical device compliance, documentation, and audits, ensuring adherence to FDA and ISO standards while collaborating across teams for...

Elevate your career as you ensure regulatory compliance in product development and manufacturing. Collaborate with project teams and guide submissions to domestic and international agencies while main...

Shape regulatory strategies by ensuring product compliance with domestic and international standards. Collaborate with cross-functional teams to facilitate approvals and navigate complexities in quali...

Lead regulatory initiatives by managing product development, compliance, and international registrations for in vitro diagnostics. Collaborate with global teams to ensure audit readiness and uphold la...

Engage in regulatory affairs to support product development, IVDR implementation, and global registrations. You'll contribute to compliance processes and cross-functional collaboration to ensure audit...

Champion regulatory strategies and submissions for global medical products, ensuring compliance across major markets while leading cross-functional teams and driving process improvements in a collabor...

Join a team that's shaping regulatory strategies in biopharmaceuticals. This role involves leading regulatory submissions and collaborating across project teams to ensure compliance while advancing co...

Provide comprehensive Regulatory Affairs support to ensure full compliance with U.S. FDA medical device regulations and international standards, facilitating product submissions and ongoing industry c...

Join a team that's shaping global regulatory strategies for innovative medical devices. Leverage your expertise in Software as a Medical Device (SaMD) to make impactful submissions and ensure complian...

Transform the future of diabetes care by guiding innovative medical devices through regulatory pathways, influencing product strategies, and ensuring compliance with global regulations while collabora...

Manage site-level regulatory operations for clinical trials, ensuring compliance with U.S. regulations. Collaborate with cross-functional teams and provide guidance for regulatory submissions, fosteri...

Transform Quality Systems by analyzing data and developing impactful executive presentations. Collaborate with global teams to support QMS processes, ensuring timely delivery of insights for managemen...

Shape your career by supporting regulatory compliance for clinical investigations and product distribution worldwide. Contribute to approvals and quality standards in a collaborative environment while...

Join an innovative team as a Clinical Affairs Specialist, where you'll develop strategies, improve processes, and ensure compliance in a dynamic, supportive environment dedicated to advancing clinical...

Lead critical clinical strategies and ensure regulatory compliance while collaborating across teams to uphold data integrity and support product development initiatives in a dynamic environment...

Partner with us to ensure seamless FTZ operations and compliance for cell therapy logistics. You'll manage inventory integrity and align cross-functional teams to support critical patient material shi...

Join a team that's dedicated to enhancing healthcare compliance. This role requires expertise in regulations and standards, managing projects, and fostering team growth while ensuring client facilitie...

Drive global regulatory strategy for medical imaging products, ensuring compliance across the software development lifecycle. Lead a dynamic team, engaging with cross-functional partners and regulator...

Join a dynamic team and lead regulatory strategies for in vitro diagnostics, ensuring compliance and successful submissions while collaborating cross-functionally. Manage project timelines and mentor...

Lead the charge in regulatory affairs across dietary supplements and consumer health products. Drive strategy, ensure compliance, and foster collaboration with key functions to navigate FDA and FTC re...

Elevate regulatory compliance across global markets by leading impactful submissions and managing complex documentation. Partner with technical teams to ensure product adherence to quality standards i...

Drive regulatory compliance by preparing FDA submissions, maintaining global registrations, and collaborating with technical teams. Guide audits and develop SOPs to ensure product quality and adherenc...

Join a team that's central to driving compliance in cosmetics and OTC products. You'll collaborate cross-functionally to support regulatory registration processes in the US and Canada, ensuring timely...