Senior Regulatory Affairs Specialist Jobs

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...

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 our team as a regulatory affairs expert, managing global submissions, driving product development, and ensuring compliance with regulatory standards for medical devices to foster innovation and s...

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...

Drive compliance and regulatory strategy by evaluating product changes, managing post-market activities, and coordinating across departments to ensure adherence to global regulations, supporting safet...

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...

Empower global product registration by managing regulatory submissions, collaborating across teams, and ensuring compliance with market regulations. Lead initiatives that drive strategic growth while...

Unlock potential by leading global regulatory submissions and strategic compliance initiatives, ensuring adherence to international standards while mentoring specialists and optimizing project timelin...

Join a dynamic team to navigate regulatory processes for medical devices, develop strategies for U.S. and Canadian markets, and lead submissions. Collaborate with cross-functional teams to ensure comp...

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...

Grow your career with a dynamic team managing regulatory projects for IVD devices. Engage in global compliance, product development, and ensure adherence to medical device regulations. Collaborate wit...

Lead the charge in preparing precise regulatory submissions, ensuring compliance for drugs and devices. Collaborate with agencies like Health Canada and FDA while managing regulatory documents and str...

Transform regulatory landscapes by delivering strategic support for digital health and medical device submissions. Collaborate with teams to ensure compliance and enhance project success through your...

Empower effective regulatory strategy development for HCT/P and combination products. Lead submissions and audits while ensuring compliance with FDA standards. Collaborate with teams to foster excelle...

Drive regulatory excellence by leading pre-/post-market activities for medical devices, developing strategies, performing assessments, and coordinating submissions for successful product lifecycle man...

Advance regulatory excellence by guiding Phase 2-4 clinical trials. Collaborate with sites and stakeholders to ensure compliance, resolving complex issues efficiently while enhancing processes across...

Join a team that's committed to advancing clinical trials by overseeing regulatory operations and ensuring compliance across multiple studies within a dynamic environment, while collaborating with var...

Drive regulatory excellence by managing compliance for Phase 2-4 clinical trials. Collaborate with stakeholders, mentor teams, and enhance processes to ensure research integrity and operational succes...

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...

Unlock potential by serving as a regulatory expert, supporting strategic business development and compliance activities across the product lifecycle while collaborating with cross-functional teams...

Provide regulatory expertise by preparing submissions, ensuring compliance, and collaborating with teams to maintain quality guidelines, supporting product development efforts and compliance with glob...

Engage in regulatory leadership for complex, federally regulated clinical trials. Oversee study start-up, compliance, and mentoring while ensuring adherence to federal regulations and best practices f...

Drive regulatory success by managing complex submissions globally, ensuring compliance with diverse requirements. Collaborate with cross-functional teams to guide product development and maintain up-t...

Pioneer regulatory strategies for medical devices, ensuring timely global approvals, compliance, and quality. Collaborate across teams, mentor peers, and tackle complex submissions for US, EU, and bey...

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...