Senior Regulatory Affairs Specialist Jobs in Chicago, IL

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...

Engage in the timely review and submission of Medical Device Reports, ensuring compliance with regulations while collaborating with cross-functional teams to enhance documentation and quality processe...

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

Lead regulatory compliance programs ensuring inspection readiness and proactive risk management across cross-functional teams. Monitor compliance health, manage data quality, and drive improvements al...

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...

Serve as a strategic regulatory leader, guiding nonclinical drug development and ensuring compliance for successful clinical entry and regulatory submissions, collaborating with cross-functional teams...

Shape the future of medical devices by leading regulatory CMC strategies, ensuring compliance and collaboration across teams to drive the development of innovative combination products for patients wo...

Transform compliance through expertise in HR regulations, policy management, and training. Support a culture of accountability while navigating multi-state employment laws across diverse teams, ensuri...

Shape innovations in insurance product development by managing regulatory compliance, enhancing product offerings, and fostering collaborative relationships across underwriting business units...

Advance your career by driving regulatory strategies for innovative pharmaceutical products in a dynamic environment. Oversee critical submissions, collaborate with cross-functional teams, and influen...

Empower your career by providing regulatory support for global electronic submissions of medical devices. Collaborate with teams to ensure compliance, organize submissions, and track deliverables in a...

Accelerate regulatory strategy development for oncology products, leading global initiatives to secure IND/CTA approvals and marketing applications. Collaborate with cross-functional teams to navigate...

Champion regulatory excellence by leading postmarket strategies for product compliance, driving collaboration across teams to ensure timely submissions and navigate complex regulatory landscapes for c...

Elevate regulatory strategies by collaborating across teams to ensure compliance and quality in submissions. Develop proactive risk assessments and maintain knowledge of CMC regulatory environments fo...

Lead and enhance clinical monitoring operations by managing teams, ensuring compliance, and delivering quality results to drive clinical trial success while developing talent and innovative solutions...

Strategize regulatory compliance and decision-making for complex products while leading cross-functional teams. Ensure lifecycle management and align strategies with business objectives to mitigate ri...

Drive global CMC regulatory strategies and submissions for clinical and commercial products. Collaborate cross-functionally to ensure compliance, lifecycle management, and timely delivery of high-qual...

Innovate the future of regulatory labeling by driving strategies across global teams, ensuring compliance and quality at all stages of product development while collaborating with key stakeholders to...

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...

Champion the validation of cutting-edge lab instrumentation while collaborating with diverse teams to ensure customer readiness and operational excellence. Your expertise will drive quality and compli...

Drive innovation by leading cross-functional R&D projects from concept through to commercialization of medical device products, ensuring compliance and collaboration with diverse teams to bring effect...

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...

Analyze and drive regulatory CMC strategies for investigational and commercial products, collaborating with cross-functional teams to ensure compliance and success in a dynamic biotech environment. Yo...

Transform regulatory writing by leading complex submissions, mentoring teams, and ensuring compliance. Drive innovation and improve processes while collaborating across teams to enhance product succes...