Regulatory Affairs Specialist Jobs

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...

Collaborate with cross-functional teams to integrate regulatory knowledge throughout the product lifecycle, ensuring compliance and effective project coordination for market authorizations in the medi...

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...

Join a dynamic team ensuring global regulatory approvals for life-saving medical technologies. You will manage complex submissions, compliance, and communication with regulatory agencies to aid in the...

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

Support regulatory compliance by managing submissions and liaising with agencies. Contribute to product development and post-market activities, ensuring all regulatory requirements are met for sustain...

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...

Deliver innovative regulatory support for animal health products, ensuring compliance with USDA regulations. Collaborate with cross-functional teams while managing multiple projects to maintain produc...

Elevate your career by supporting regulatory compliance efforts for animal health products. Collaborate cross-functionally to manage project timelines and contribute to successful submissions under US...

Transform regulatory processes by preparing and coordinating submissions for global approvals, ensuring compliance and quality for medical devices that enhance patient care worldwide...

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...

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...

Tackle regulatory challenges by ensuring compliance and supporting submissions in the healthcare and biotechnology sectors. Collaborate with diverse teams to facilitate product approvals while monitor...

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...

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...

Drive global regulatory compliance and product registration for medical devices. Coordinate submissions and maintain documentation while collaborating with internal and external stakeholders to ensure...

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...