Regulatory Affairs Manager Jobs in Chicago, IL

Manage regulatory submissions and compliance for medical devices. Collaborate across departments to ensure adherence to standards, support audits, and maintain quality throughout clinical processes an...

Lead and innovate within our centralized analytics team, driving automation and data governance strategies across multiple functions to enhance operational efficiency and decision-making in a dynamic...

Drive regulatory strategy by collaborating cross-functionally to influence promotional activities, ensuring compliance while optimizing risk management for impactful business decisions across a dedica...

Drive global regulatory labeling initiatives, ensuring compliance and quality of documentation across diverse markets. Lead strategic governance, influence policies, and collaborate cross-functionally...

Drive enterprise Quality and Regulatory governance for U.S. operations, ensuring compliance with FDA regulations and overseeing manufacturing quality in the therapeutic radiopharmaceutical sector whil...

Shape the future of GMP readiness by developing strategic quality systems and roadmaps, ensuring efficient market entry for innovative cell-based assay products. Guide teams in compliance, regulatory...

Unlock potential by driving regulatory submissions and managing documentation. Collaborate with global teams to align on strategies, ensuring compliance and effective communication while fostering a c...

Transform government pricing strategies by managing client relations and ensuring accurate federal drug price calculations while mentoring a team of analysts and providing expert guidance in complianc...

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

Unlock potential by leading compliance in digital regulatory assurance through automation and AI. Collaborate across teams to optimize IT operations, drive continuous improvements, and ensure adherenc...

Join a team dedicated to ensuring drug quality compliance by performing data integrity audits, assessing adherence to FDA standards, and providing actionable recommendations to enhance regulatory deci...

Lead the charge in regulatory affairs for medical device development, driving compliance and strategic submission processes. Collaborate with global teams to ensure timely project execution while main...

Empower innovation in quality compliance by overseeing GCP activities, conducting audits, managing regulatory inspections, and ensuring effective risk mitigation strategies throughout clinical develop...

Lead major external reviews and internal audit projects, ensuring compliance and efficiency. Manage auditing processes, supervise staff, and train on best practices to enhance operational success and...

Join a team that's leading major audits and projects, optimizing internal operations while ensuring compliance. Utilize your expertise in auditing and project management to drive improvements in the h...

Pioneer a robust Quality Management System by ensuring compliance with FAA, AS9100, and Nadcap standards. Lead cross-functional teams to drive quality initiatives that enhance product integrity and al...

Collaborate with clients and teams to manage projects, expectations, and delivery, ensuring high standards and strategic growth in a fast-paced medical affairs environment. Leverage experience to iden...

Join a strategic leadership role that executes regulatory strategies globally, overseeing complex submissions and driving cross-functional collaboration to ensure successful market access and complian...

Contribute to regulatory excellence by coordinating U.S. submissions, ensuring compliance with FDA standards, and maintaining vital documentation for the Obesity Therapeutic Area, while collaborating...

Lead the charge in developing global regulatory strategies for clinical programs. Manage regulatory operations for product lifecycle while collaborating with cross-functional teams to ensure successfu...

Create impactful regulatory strategies that advance global product development, ensuring compliance with medical device regulations and driving business expansion while collaborating cross-functionall...

Lead the charge in global regulatory strategies for innovative medical devices, driving project success from registration to compliance. Collaborate across teams to enhance healthcare technologies and...

Advance patient safety operations by managing a team, ensuring compliance, and enhancing pharmacovigilance processes while fostering a collaborative environment for continuous improvement and innovati...

Champion regulatory excellence by guiding project teams, developing global strategies, managing submissions, and ensuring compliance with FDA and international regulations while navigating complex env...

Join a team that's dedicated to advancing regulatory strategies for innovative SaMD products. Collaborate cross-functionally to drive compliance, manage documentation, and ensure readiness for audits...