Regulatory Affairs Specialist Jobs in Santa Ana, CA

Lead regulatory permitting strategies and ensure compliance with environmental regulations, managing projects from inception to completion while fostering strong client and agency relationships...

Collaborate to drive regulatory strategy and compliance for medical devices, ensuring alignment with business goals. Engage cross-functionally to meet FDA and international standards, supporting produ...

Lead the charge in developing global regulatory strategies for clinical programs. Manage regulatory operations for product lifecycle while collaborating with cross-functional teams to ensure successfu...

Support the Quality Management System by reviewing and approving key documentation, ensuring compliance with regulations. Champion best practices in discrepancy reporting and CAPA processes while coll...

Serve as a strategic regulatory leader, guiding nonclinical drug development and ensuring compliance for successful clinical entry and regulatory submissions, collaborating with cross-functional teams...

Bring your expertise to the regulatory affairs realm, overseeing advertising and promotion compliance, guiding teams, and influencing industry standards. Lead initiatives that ensure products meet leg...

Optimize regulatory strategies for robotic surgical instruments, ensuring compliance and market access. Lead cross-functional teams, prepare vital submissions, and drive innovative product development...

Champion regulatory excellence by leading postmarket strategies for product compliance, driving collaboration across teams to ensure timely submissions and navigate complex regulatory landscapes for c...

Transform compliance through expertise in HR regulations, policy management, and training. Support a culture of accountability while navigating multi-state employment laws across diverse teams, ensuri...

Unlock potential by leading regulatory strategies for innovative medical devices. Collaborate with teams to ensure compliance, execute FDA submissions, manage project timelines, and establish processe...

Join a team that's at the forefront of developing regulatory strategies for medical devices. Drive global compliance and foster a culture of regulatory excellence while collaborating with diverse team...

Lead global regulatory strategies for oncology programs, ensuring compliance and effectively interacting with regulatory agencies for product approvals in late-stage development...

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...

Join a team that's shaping regulatory strategies for US and Canada markets, ensuring compliance for therapeutic products through effective planning and execution. Collaborate across functions while in...

Join a pivotal role in regulatory affairs, guiding promotional materials in compliance with FDA and provincial guidelines in a dynamic, remote environment. Lead the Materials Review Committee and shap...

Drive global CMC strategy for transformative cell and gene therapies, ensuring seamless regulatory pathways and efficient product approvals through collaborative leadership and strategic risk manageme...

Lead the charge in regulatory strategy for US and Canada, ensuring compliance for medical devices while collaborating across teams to navigate complex regulations and drive product commercialization...

Unlock potential by managing the equipment lifecycle and compliance for quality systems. Collaborate cross-functionally to ensure all devices are audit-ready while innovating processes to streamline o...

Pioneer global regulatory strategies, driving compliance solutions that ensure timely access to life-saving products while leading complex initiatives across diverse teams to enhance patient outcomes...

Shape the future of regulatory strategy by leading cross-functional teams, driving innovative development strategies, and providing regulatory thought leadership to ensure compliance and accelerate pr...

Accelerate your impact by winning high-value, complex opportunities through innovative workflow design and technical expertise, while shaping market direction and influencing strategic commercial deci...

Join as a Clinical Research Associate to oversee critical monitoring tasks across diverse clinical studies. Ensure high-quality standards while facilitating communication between project teams and sit...

Advance regulatory strategies and oversight for global clinical trials. Support submission preparation, manage CRO interactions, and collaborate cross-functionally to navigate regulatory challenges an...

Optimize validation processes by ensuring compliance with GMP regulations and quality standards. Leverage your QA expertise to manage and approve essential documentation, while fostering cross-functio...

Transform regulatory writing by leading complex submissions, mentoring teams, and ensuring compliance. Drive innovation and improve processes while collaborating across teams to enhance product succes...