Senior Regulatory Affairs Specialist Jobs in Minnetonka, MN

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 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...

Join a team that shapes global regulatory strategy in a fast-paced environment. You will lead comprehensive regulatory plans, ensuring alignment and execution from development to post-marketing, impac...

Reimagine Regulatory Affairs by leading complex outsourcing programs and driving client success. Utilize deep expertise in strategy and operations to manage projects, mentor teams, and deliver tailore...

Champion regulatory excellence by developing global strategies for product registration and ensuring compliance across markets. Collaborate with cross-functional teams to secure timely approvals and s...

Champion regulatory strategies and submissions for global medical products, ensuring compliance across major markets while leading cross-functional teams and driving process improvements in a collabor...

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...

Join a dynamic legal team to optimize regulatory processes, ensuring compliance with state and federal laws while collaborating with various departments. Experience a flexible remote work environment...

Manage regulatory strategies and submissions for medical devices, ensuring compliance with global standards. Collaborate with cross-functional teams and regulatory agencies to drive successful outcome...

Unlock the potential of real-world data by guiding clinical research efforts. Collaborate cross-functionally to execute impactful studies and drive long-term strategies in Urology, enhancing the evide...

Join our dynamic Urology team as a Senior Clinical Research Specialist, guiding real-world evidence strategies to enhance clinical research activities, improve patient outcomes, and support innovative...

Engage with a dynamic team to facilitate regulatory operations for novel therapeutics. Drive submissions to FDA/CVM while collaborating across multidisciplinary teams to set new regulatory standards i...

Shape the future of regulatory strategy by leading projects that ensure compliance and market access. Drive collaboration across teams while managing processes for development and post-approval phases...

Engage with cross-functional teams to ensure regulatory compliance for Expanded Access Programs. Drive essential strategies and submissions while staying aligned with global legislation, impacting pat...

Lead the charge in transforming global regulatory strategies into successful outcomes. Oversee regulatory activities and empower teams to ensure quality compliance, timely delivery, and robust cross-f...

Join our team to lead regulatory strategies across major programs, driving impactful submissions and fostering collaboration within a challenging and dynamic environment. Embrace the opportunity to in...

Join a team that's shaping the future of active implantable medical devices by supporting clinical evaluations and regulatory submissions. Collaborate across disciplines to ensure compliance with EU a...

Optimize quality systems by analyzing standards, documenting issues, and enhancing processes. Collaborate closely with teams to verify components, ensure compliance, and drive improvements while effec...

Provide comprehensive Regulatory Affairs support to ensure full compliance with U.S. FDA medical device regulations and international standards, facilitating product submissions and ongoing industry c...

Deliver impactful CMC regulatory support for IND/CTA development and maintenance, ensuring compliance and completeness across submissions while leading cross-functional collaboration and strategically...

Drive compliance excellence by overseeing regulatory adherence for complex benefit products. Collaborate with cross-functional teams, conduct risk assessments for innovations, and support escalations...

Lead global regulatory strategies for oncology programs, ensuring compliance and effectively interacting with regulatory agencies for product approvals in late-stage development...

Accelerate your impact by winning high-value, complex opportunities through innovative workflow design and technical expertise, while shaping market direction and influencing strategic commercial deci...

Unlock the power of regulatory insights! Lead comprehensive monitoring and analysis of regulatory developments, providing actionable intelligence to guide business strategy and decision-making across...

Take ownership of regulatory strategies and policies for medical devices, collaborating with cross-functional teams to ensure compliance and optimize operations in a dynamic healthcare environment. Ma...