Regulatory Specialist Jobs

Reimagine global compliance strategies as you guide regulatory submissions, assess product impacts, and collaborate across teams to ensure adherence to medical device regulations while enhancing quali...

Join an innovative team driving environmental planning and permit compliance for large-scale projects. Engage in vital NEPA documentation and coordination with agencies to ensure successful project ex...

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...

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

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...

Champion environmental progress by leading NEPA documentation and permit applications for large capital projects. Your expertise will drive collaboration across teams to navigate regulatory hurdles an...

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...

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...

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...

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...

Drive regulatory activities for Animal Health products, ensuring compliance and accurate submissions, while collaborating with cross-functional teams to manage labeling, lifecycle, and operational pro...

Lead the charge in environmental compliance and sustainability across Americas manufacturing sites. Collaborate with teams to ensure regulatory adherence, enhance performance, and promote a culture of...

Champion environmental compliance across multiple manufacturing sites, driving sustainability initiatives and risk reduction while enhancing compliance programs and fostering a culture of stewardship...

Join a team that's dedicated to enhancing import compliance by analyzing data, investigating discrepancies, and collaborating with customs brokers. Your role will ensure accurate entry processing and...

Join a team that's pivotal in enhancing customs compliance and duty recovery. As a Post Entry Corrections Analyst II, you'll analyze import transactions, collaborate with various stakeholders, and dri...

Join the Trade Compliance team and play a key role in ensuring import compliance, identifying duty recovery opportunities while collaborating with customs brokers and stakeholders to enhance DTNA's gl...

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...

Elevate regulatory compliance processes by coordinating IRB submissions and ensuring adherence to GCP, FDA regulations, and internal protocols. Collaborate with cross-functional teams to maintain docu...

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...

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

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...

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...