Regulatory Specialist Jobs in Irvine, CA

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

Accelerate regulatory compliance projects by preparing permits, managing habitat restoration, and overseeing environmental impact assessments. Collaborate closely with clients and multidisciplinary te...

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...

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 regulatory excellence by overseeing compliance for product claims, labeling, and ingredient evaluations. Collaborate with teams to ensure timely submissions and strategic solutions for regulator...

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...

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...

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...

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...

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...

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...

Grow your career with a pivotal role in delivering engaging regulatory education to the insurance sector while building client relationships and collaborating with a dedicated team to ensure complianc...

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...

Drive regulatory strategy by guiding product development teams, ensuring compliance, and preparing documentation for global submissions. Monitor regulations and assess their impact, while fostering so...

Drive impactful environmental projects by applying your RCRA expertise. Lead multidisciplinary teams, ensure regulatory compliance, and deliver innovative solutions for clients in industrial, commerci...

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 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...

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...

Manage regulatory processes for advanced nuclear technology deployment, leading submissions and timelines while mentoring junior staff. Collaborate with stakeholders and regulators to streamline commu...

Contribute to the MLR process by coordinating reviews, ensuring compliance, and driving improvements across Marketing, Medical Affairs, and Corporate Communications while collaborating with internal t...

Transform global regulatory processes by leading approvals, strategizing submissions, and ensuring compliance for medical devices across diverse markets while collaborating with teams and serving as a...

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...

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...