Regulatory Affairs Specialist Jobs

Shape the future of regulatory excellence by managing global submissions, ensuring compliance across the drug development lifecycle, and collaborating across teams to facilitate strong health authorit...

Shape the future of regulatory strategy and execution, driving high-quality submissions and interactions with global health authorities throughout the drug development lifecycle, ensuring adherence to...

Take ownership of quality operations by ensuring compliance through batch record review and supplier oversight. Collaborate with cross-functional teams to support clinical and commercial product quali...

Transform clinical trial management by maintaining essential documents and trackers, ensuring compliance with regulations, and supporting study teams throughout trial phases. Contribute to efficient o...

Join a team that's dedicated to optimizing contracts and financial strategies in a fast-paced medical sales environment, ensuring compliance and maximizing business performance while driving analytica...

Shape the global Advertising & Promotional Compliance strategy, leading regulatory efforts and ensuring compliance for promotional materials while collaborating with cross-functional teams to enhance...

Manage end-to-end product stewardship and regulatory services for a global chemical ink portfolio. Collaborate cross-functionally to ensure compliance and market access while maintaining sustainabilit...

Drive excellence in quality compliance by leading product quality reviews, performing audits, and ensuring regulatory adherence while fostering collaboration across departments to uphold safety and qu...

Join a team that enhances customer satisfaction through clinical promotion and training of cutting-edge imaging technologies in medical and veterinary systems, leveraging your expertise for impactful...

Unlock potential by joining a dynamic Quality Assurance team, overseeing validation projects, collaborating with cross-functional teams, and ensuring compliance with ISO and GMP regulations in a fast...

Contribute to quality assurance and validation processes for medical devices, ensuring compliance with ISO and GMP regulations. Collaborate cross-functionally to support process development and techni...

Lead the charge in developing global regulatory strategies to secure market approval for products in assigned therapeutic areas, guiding cross-functional teams and ensuring compliance throughout the p...

Analyze and document medical device reports for regulatory compliance, ensuring they meet international standards. Collaborate with cross-functional teams to drive improvements in processes and suppor...

Accelerate progress at our Diabetes Care division by ensuring compliance with medical reporting regulations, documenting medical events, and collaborating with cross-functional teams to enhance produc...

Champion cross-functional collaboration to drive quality assurance practices and enhance product development. Lead Design Assurance initiatives, ensuring compliance with regulatory standards while men...

Drive regulatory strategy to ensure successful US drug and biological product development and approval. Collaborate with cross-functional teams to achieve compliance, maintain communication, and suppo...

Transform clinical research through effective site management and monitoring. Engage with study teams to uphold regulations and ensure quality in trials. Leverage your expertise in trials for impactfu...

Accelerate your impact in quality assurance by overseeing CMC operations, managing batch releases, and ensuring compliance. Collaborate with teams to uphold regulatory standards while enhancing your e...

Support pharmaceutical and chemical projects by leading process design, scale-up, and optimization initiatives. Engage with clients and mentor junior engineers to deliver high-quality outputs aligning...

Lead the charge in small molecule manufacturing process design and optimization. Engage clients, manage projects, mentor junior staff, and ensure compliance with industry regulations across diverse ph...

Join us to optimize and support critical pharmaceutical applications such as Veeva Vault and CRM. Collaborate with cross-functional teams to improve operations, enhance system functionality, and ensur...

Lead the charge in transforming FDA insights into proactive compliance solutions. Engage with clients to identify risks, drive quality improvements, and mentor teams, all in a collaborative environmen...

Join a team that defines the global strategy for CMC regulatory submissions, ensuring timely approvals and effective communication within cross-functional teams to enhance patient outcomes and drive s...

Grow your career with our Compliance Specialist role, where you will lead compliance efforts, conduct audits, and collaborate on environmental projects across various programs, ensuring adherence to i...

Take ownership of compliance by monitoring industry regulations, resolving case activities, and collaborating across teams to ensure adherence to standards, ultimately maintaining the organization's r...