Regulatory Affairs Specialist Jobs

Take ownership of global post-market regulatory compliance activities. Collaborate across teams to ensure adherence to U.S. and international regulations while driving continuous improvements in incid...

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

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...

Unlock potential by driving regulatory strategies for innovative medical devices. Collaborate across teams to secure product approvals while ensuring compliance with global regulations and quality sta...

Join a team that manages global regulatory submissions across diverse markets. Enhance compliance through documentation, support audits, and collaborate with cross-functional teams to ensure product m...

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...

Join a dynamic team to ensure compliance and regulatory excellence in documentation and submissions. Collaborate on vital regulatory affairs projects while engaging with key regulatory agencies to fac...

Help us ensure compliance and drive success in medical device regulatory affairs, maintaining licenses and submissions across multiple jurisdictions while collaborating with teams to uphold standards...

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...

Join our dynamic team to lead international regulatory submissions for innovative digital health technologies, ensuring compliance across global markets and collaborating cross-functionally for succes...

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...

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...

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...

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...

Lead the charge in enhancing regulatory frameworks for product compliance, ensuring quality system effectiveness, and supporting innovative medical diagnostics. Collaborate cross-functionally to meet...

Elevate product safety and compliance as a key player in regulatory affairs, ensuring adherence to local and international standards for pharmaceutical products. Collaborate with diverse teams to navi...

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

Join a team that's pivotal in regulatory strategy, independently preparing eCTD submissions, and assessing promotional materials for compliance while collaborating with cross-functional teams to ensur...

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...

Transform regulatory compliance by leading submissions and strategies for high-risk medical devices. Collaborate with cross-functional teams to ensure adherence to FDA and Health Canada standards thro...

Drive the compliance of labeling and promotional materials to enhance regulatory standards while preparing eCTD submissions and collaborating with cross-functional teams on product development and reg...

Unlock potential by driving regulatory success for animal health products. Collaborate cross-functionally to manage regulatory submissions, compliance, and lifecycle support, ensuring timely delivery...

Shape the future of drug development by leading nonclinical regulatory strategies and engagements. Collaborate with multidisciplinary teams and clients to drive clinical progress, ensuring compliance...

Elevate your expertise by joining a dynamic team that drives nonclinical regulatory strategies for drug, biologic, and vaccine development, ensuring advancement from discovery to clinical approval whi...