Regulatory Affairs Manager Jobs

Champion regulatory excellence by leading global submissions and compliance for medical devices. Collaborate with cross-functional teams to ensure adherence to standards while driving strategic initia...

Lead regulatory strategies to ensure global product compliance and approval. Collaborate with cross-functional teams to drive successful submissions and maintain regulatory standards, while fostering...

Manage regulatory strategies for global product approvals, ensuring compliance and collaboration across teams. Lead submission activities for medical devices, fostering a high-performance culture whil...

Lead the charge in developing regulatory strategies for Canadian projects, ensuring compliance and collaboration across teams to drive successful product development and submissions in a dynamic, scie...

Lead the charge in regulatory operations for clinical trials, ensuring compliance and excellence from startup to closeout. Mentor a team of professionals while managing IRB submissions, documentation...

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...

Join our dynamic Regulatory Affairs team to drive compliance and strategy for product launches across multiple markets. Collaborate cross-functionally to ensure regulatory adherence and support innova...

Elevate your career by leading regulatory strategy and compliance for diverse product portfolios. Collaborate cross-functionally to ensure successful product launches and ongoing compliance in domesti...

Transform regulatory strategies for rare disease and cardio-pulmonary drug-device programs. Collaborate with cross-functional teams to ensure compliance and drive successful submissions globally, supp...

Lead the charge in regulatory compliance for medical devices, managing submissions and strategies to ensure timely approvals and market access while collaborating with cross-functional teams to enhanc...

Lead the New Product Development (NPD) submission process, ensuring strategic alignment and risk mitigation. Collaborate with internal teams and partners to optimize regulatory submissions and respons...

Accelerate progress at the forefront of New Product Development by leading regulatory submissions, ensuring compliance, and collaborating with internal and external teams to drive successful product l...

Transform global entity management by coordinating across Finance, HR, and Legal. Ensure compliance, maintain corporate records, and build scalable processes as we expand internationally. Drive operat...

Lead the charge in regulatory operations, ensuring compliance and quality for medical devices. Oversee documentation systems, manage global submissions, and guide teams to achieve project goals while...

Transform regulatory operations by leading teams to ensure compliance and quality in medical device submissions. Oversee projects, manage documentation systems, and drive continuous improvement to mee...

Lead the charge in global regulatory submissions, managing U.S. INDs and ex-U.S. CTAs. Collaborate cross-functionally to develop strategies, ensure compliance, and drive timely approvals in a fast-pac...

Join a team that's shaping global regulatory strategies, managing U.S. and ex-U.S. submissions, and ensuring compliance with FDA and EU regulations. Leverage your expertise to drive impactful regulato...

Join a team that's dedicated to ensuring compliance in global medical device registrations. You'll execute regulatory strategies, prepare essential documents, and collaborate with cross-functional tea...

Drive global regulatory strategies for IVD test systems, ensuring compliance and successful market authorization. Collaborate with cross-functional teams to support product development and lifecycle m...

Drive regulatory intelligence initiatives to ensure compliance and support clinical research. Collaborate with experts to assess regulatory changes, track global guidelines, and enhance impact assessm...

Join a team that's shaping the future of medical devices and digital health. As a Regulatory Affairs Specialist, you'll drive regulatory strategies for innovative technologies, ensuring compliance and...

Elevate progress at the forefront of CMC Regulatory Affairs, leading strategies and compliance for biologics. Collaborate with global teams to ensure regulatory excellence throughout development and p...

Accelerate progress at the forefront of CMC Regulatory Affairs, leading strategies and compliance for biologics. Collaborate with global teams to ensure regulatory excellence throughout product develo...

Elevate your career by leading regulatory strategy and compliance for biologic products. Collaborate with cross-functional teams to ensure adherence to global regulations and drive efficiency in CMC p...

Champion CMC regulatory strategies for biologics, ensuring compliance and efficiency in submissions, interactions, and process improvements while leading cross-functional teams to navigate complex reg...