Regulatory Affairs Specialist Jobs in Lake Forest, 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...

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...

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...

Drive regulatory compliance by implementing quality systems and supporting product development. Collaborate with teams to ensure effective documentation, submissions, and strategies while analyzing pr...

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...

Join a dynamic team as you lead regulatory compliance initiatives, collaborating across departments to navigate complex medical device regulations. Your expertise will ensure product safety and effica...

Join a team that shapes global regulatory strategy in a fast-paced environment. You will lead comprehensive regulatory plans, ensuring alignment and execution from development to post-marketing, impac...

Drive regulatory compliance by supporting clinical protocol submissions, training documentation, and communication with internal teams to ensure timely and accurate execution of clinical projects and...

Reimagine Regulatory Affairs by leading complex outsourcing programs and driving client success. Utilize deep expertise in strategy and operations to manage projects, mentor teams, and deliver tailore...

Shape the future of regulatory compliance by leading lifecycle management projects, coordinating approvals, and developing strategies for new medical devices, while fostering relationships with teams...

Oversee regulatory initiatives ensuring compliance for medical devices. Collaborate with cross-functional teams to achieve regulatory clearances and support product development while managing internat...

Shape the future of regulatory strategy by leading projects that ensure compliance and market access. Drive collaboration across teams while managing processes for development and post-approval phases...

Join a team that’s shaping the future of food compliance by ensuring labeling accuracy and regulatory adherence across multiple regions, fostering collaboration across functions to enhance product int...

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...

Optimize regulatory compliance processes to ensure product quality and adherence to global standards while coordinating submissions and managing cross-functional teams for effective risk management...

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...

Engage with cross-functional teams to ensure regulatory compliance for Expanded Access Programs. Drive essential strategies and submissions while staying aligned with global legislation, impacting pat...

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...

Lead the charge in transforming global regulatory strategies into successful outcomes. Oversee regulatory activities and empower teams to ensure quality compliance, timely delivery, and robust cross-f...

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...

Drive the transformation of clinical research operations by leading the implementation of an innovative eRegulatory platform, ensuring compliance and optimizing efficiencies. Collaborate with diverse...

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...

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...

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...

Transform the regulatory landscape by developing and executing strategic plans for market and development products in the US and Canada, ensuring compliance and successful commercialization while navi...