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...

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...

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

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...

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...

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...

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...

Engage in international regulatory affairs, driving submissions, registrations, and lifecycle management for medical devices in the UK, Japan, and Latin America. Collaborate with regulatory bodies and...

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...

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...

Elevate your career by leading regulatory strategy for high-risk medical devices. Collaborate with teams to ensure compliance, prepare submissions, and maintain product registrations. Your expertise w...

Join our dynamic team to drive regulatory compliance, support product safety initiatives, and collaborate across functions to ensure adherence to global regulations. Your expertise will be crucial in...

Lead compliance and regulatory activities for medical devices, ensuring adherence to FDA and international standards while managing risk assessments and product recalls. Collaborate cross-functionally...

Optimize compliance by managing regulatory submissions and providing strategic guidance for product development and market expansion across diverse global markets...

Shape the future of regulatory affairs by driving compliance and strategic planning for global product registrations. Collaborate cross-functionally to enhance processes and ensure successful submissi...