Regulatory Affairs Manager Jobs in Thousand Oaks, CA

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 strategies and oversee compliance for investigational therapies. Work cross-functionally to ensure timely regulatory filings and maintain vendor relationships, contributing to clinica...

Elevate the regulatory landscape by guiding strategic promotional communications for Oncology products. Shape impactful messaging while ensuring compliance and aligning with evolving regulations and F...

Shape compliance strategies in regulatory affairs, overseeing promotional materials and interactions with FDA. Lead cross-functional reviews, ensuring adherence to guidelines while supporting business...

Join a team that's dedicated to regulatory compliance and product stewardship, leading efforts across markets in North America. Oversee daily operations, drive continuous improvement, and cultivate a...

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...

Champion regulatory excellence for high-risk implantable devices internationally, engaging with global regulators, driving compliance, and leading cross-functional teams to ensure successful market ac...

Help us shape the future of clinical trials by providing regulatory guidance and maintaining compliance. Collaborate within cross-functional teams to ensure successful submissions and uphold industry...

Champion regulatory excellence in CMC for innovative cell therapies, enhancing submission strategies and compliance. Collaborate with cross-functional teams on lentiviral vector processes to drive adv...

Oversee CMC regulatory functions, ensuring compliance for lentiviral vector and cell therapy products. Collaborate with cross-functional teams to support regulatory submissions and strategies, contrib...

Shape the future of gene therapy by leading CMC regulatory efforts for cell therapies and lentiviral vectors. Collaborate across teams to ensure compliance, support regulatory submissions, and drive q...

Take ownership of regulatory affairs operations, leading teams to enhance processes within clinical trials while ensuring compliance with regulations and fostering collaboration across departments...

Lead end-to-end GCP audits globally, ensuring compliance and driving improvements in clinical studies. Collaborate with stakeholders to interpret regulations and support regulatory inspections in a dy...

Lead regulatory compliance programs ensuring inspection readiness and proactive risk management across cross-functional teams. Monitor compliance health, manage data quality, and drive improvements al...

Drive strategic initiatives that enhance quality and compliance for Early Phase Clinical Units, managing risk and compliance leads while collaborating with cross-functional teams to ensure alignment w...

Optimize regulatory strategies and compliance globally by leading cross-functional projects, guiding teams, and liaising with health authorities throughout the drug development lifecycle to ensure suc...

Discover opportunities to advance complex CMC regulatory strategies, ensuring compliance and quality across cell therapy product lifecycles. Partner with cross-functional teams, driving submissions an...

Shape complex CMC regulatory strategies for innovative cell therapy products, ensuring compliance, timely submissions, and high-quality deliverables while collaborating across diverse teams in a dynam...

Contribute to vital CMC regulatory strategies for cell therapy products, ensuring compliance and quality execution across clinical and commercial phases while collaborating with cross-functional teams...

Lead the charge in driving complex CMC regulatory activities for cell therapy products, enhancing global strategies and ensuring compliant submissions while collaborating with cross-functional teams t...

Join a team that's dedicated to ensuring compliance in promotional activities for CNS treatments while navigating regulatory pathways in a fast-paced environment. Help shape communications, drive stra...

Join a team that drives regulatory excellence for clinical development, ensuring strategic and compliant submissions. Collaborate cross-functionally to accelerate drug approval processes while oversee...

Manage regulatory submissions and compliance for medical devices. Collaborate across departments to ensure adherence to standards, support audits, and maintain quality throughout clinical processes an...

Drive regulatory strategy by collaborating cross-functionally to influence promotional activities, ensuring compliance while optimizing risk management for impactful business decisions across a dedica...

Drive global regulatory labeling initiatives, ensuring compliance and quality of documentation across diverse markets. Lead strategic governance, influence policies, and collaborate cross-functionally...