Regulatory Affairs Specialist Jobs

Elevate regulatory standards by coordinating global submissions for medical devices, ensuring compliance with U.S. and international guidelines while supporting cross-functional collaboration and stra...

Shape the future of medical devices by securing 510k and NDA approvals through strategic regulatory compliance. Collaborate cross-departmentally to streamline submissions, maintain documentation, and...

Transform regulatory strategies to ensure compliance for innovative medical devices while collaborating with cross-functional teams on product development and clinical studies. Drive timely submission...

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 leveraging your expertise in compliance and strategic assessments for medical device projects. Collaborate cross-functionally to ensure adherence to FDA and internationa...

Elevate regulatory processes by coordinating submissions for global approvals, ensuring compliance and facilitating access to vital healthcare technologies through meticulous documentation and project...

Champion process excellence in Regulatory Affairs by managing issue resolution and enhancing compliance operations. Collaborate cross-functionally to ensure inspection readiness and support effective...

Lead compliance initiatives by developing and maintaining product labeling that meets FDA and international regulations, while collaborating with cross-functional teams to support innovation and growt...

Lead the charge in ensuring compliance through expert product labeling and guidance. Collaborate with cross-functional teams to ensure labeling integrity while meeting regulatory standards and fosteri...

Join a dynamic team to drive compliance and regulatory submissions for medical devices in North America, ensuring adherence to FDA and Health Canada standards while collaborating cross-functionally to...

Engage with cross-functional teams to drive regulatory strategies and submissions for medical devices while ensuring compliance through the product lifecycle, including ongoing collaboration with dome...

Advance regulatory strategies for medical devices, managing submissions and ensuring compliance throughout the product lifecycle. Collaborate with project teams and regulatory bodies on 510(k)s, PMAs...

Join a team that's dedicated to securing regulatory approvals for innovative medical technologies, ensuring access to life-saving products worldwide while managing multiple submissions and collaborati...

Drive regulatory excellence by leading and supporting medical device compliance efforts. Utilize your expertise to facilitate product development and global market access while ensuring quality delive...

Deliver compliance leadership by coordinating regulatory deliverables for product portfolios. Monitor regulations, manage change controls, mentor team members, and ensure high-quality execution of com...

Help us shape the future of regulatory compliance by supporting submissions, approvals, and post-launch activities. Engage with cross-functional teams to ensure adherence to guidelines while managing...

Analyze regulatory landscapes to ensure compliance and facilitate product approvals across pharmaceutical and medical device sectors, collaborating with cross-functional teams to drive successful subm...

Unlock potential by guiding regulatory strategies for new and existing medical devices. Collaborate across teams to ensure compliance with global regulations while managing submissions and assessments...

Join a team that's committed to ensuring compliance with regulatory standards by managing product development and labeling processes. Collaborate with cross-functional teams to navigate regulatory lan...

Unlock potential by leading comprehensive regulatory strategies for complex devices. Act as a key expert in multiple scientific disciplines, managing priorities while ensuring compliance with global r...

Shape the future of diagnostic innovation by guiding new product development through regulatory strategies, risk assessments, and FDA submissions while collaborating with diverse teams across scientif...

Lead the charge in optimizing global regulatory affairs by supporting critical business operations and enhancing user experience through effective documentation, training, and change management, ensur...

Transform innovation in regulatory affairs by guiding development teams on compliance strategies for diagnostic devices and software. Lead submissions and risk assessments, ensuring thorough collabora...

Drive regulatory excellence in North America by leading product development and registration, ensuring compliance with EPA and state agencies, and guiding strategic initiatives within the agricultural...

Unlock potential by driving regulatory strategies for medical devices; manage submissions, ensure compliance, and support product development. This role requires a proactive approach in navigating com...